ClinVar (all) for Orgtrack (Select 508797) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1722761	NM_001360016.2(G6PD):c.821A>T (p.Glu274Val)	G6PD (E274V +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722760	NM_001360016.2(G6PD):c.820G>A (p.Glu274Lys)	G6PD (E274K +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722759	NM_001360016.2(G6PD):c.811G>C (p.Val271Leu)	G6PD (V271L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722758	NM_001360016.2(G6PD):c.770G>T (p.Arg257Leu)	G6PD (R257L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722757	NM_001360016.2(G6PD):c.[769C>A;770G>T]	G6PD (R257L +1 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722756	NM_001360016.2(G6PD):c.743G>A (p.Gly248Asp)	G6PD (G248D +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722755	NM_001360016.2(G6PD):c.739G>A (p.Gly247Arg)	G6PD (G247R +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency +1 more	GConflicting classifications of pathogenicity
Select item 1722754	NM_001360016.2(G6PD):c.737G>T (p.Arg246Leu)	G6PD (R246L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722753	NM_001360016.2(G6PD):c.121-1813del	G6PD	Deletion (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722752	NM_001360016.2(G6PD):c.725_730del (p.Gly242_Thr243del)	G6PD	Deletion (inframe_deletion)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722751	NM_001360016.2(G6PD):c.697G>C (p.Val233Leu)	G6PD (V233L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722750	NM_001360016.2(G6PD):c.695G>A (p.Cys232Tyr)	G6PD (C232Y +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722749	NM_001360016.2(G6PD):c.691G>C (p.Ala231Pro)	G6PD (A231P +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722748	NM_001360016.2(G6PD):c.683ACA[1] (p.Asn229del)	G6PD (N229del +1 more)	Microsatellite (inframe_deletion)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722747	NM_001360016.2(G6PD):c.[376A>G;680G>T]	G6PD (R227L +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722746	NM_001360016.2(G6PD):c.634A>G (p.Met212Val)	G6PD (M212V +1 more)	Single nucleotide variant (missense variant)	Malaria, susceptibility to +1 more	GConflicting classifications of pathogenicity
Select item 1722745	NM_001360016.2(G6PD):c.121-2107T>C	G6PD	Single nucleotide variant (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722744	NM_001360016.2(G6PD):c.598G>A (p.Asp200Asn)	G6PD (D200N +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722743	NM_001360016.2(G6PD):c.592C>A (p.Arg198Ser)	G6PD (R198S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722742	NM_001360016.2(G6PD):c.586A>T (p.Ile196Phe)	G6PD (I196F +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722741	NM_001360016.2(G6PD):c.585G>C (p.Gln195His)	G6PD (Q195H +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722740	NM_001360016.2(G6PD):c.573C>G (p.Phe191Leu)	G6PD (F191L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722739	NM_001360016.2(G6PD):c.[143T>C;563C>T]	G6PD (I48T +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722738	NM_001360016.2(G6PD):c.121-2679C>G	G6PD	Single nucleotide variant (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722737	NM_001360016.2(G6PD):c.527A>G (p.Asp176Gly)	G6PD (D176G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722736	NM_001360016.2(G6PD):c.485+184del	G6PD	Deletion (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722735	NM_001360016.2(G6PD):c.514C>T (p.Pro172Ser)	G6PD (P172S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722734	NM_001360016.2(G6PD):c.497G>A (p.Arg166His)	G6PD (R166H +1 more)	Single nucleotide variant (missense variant)	Malaria, susceptibility to +1 more	GPathogenic/Likely pathogenic
Select item 1722733	NM_001360016.2(G6PD):c.496C>T (p.Arg166Cys)	G6PD (R166C +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722732	NM_001360016.2(G6PD):c.488G>A (p.Gly163Asp)	G6PD (G163D +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722731	NM_001360016.2(G6PD):c.486-17del	G6PD	Deletion (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722730	NM_001360016.2(G6PD):c.486-17C>T	G6PD	Single nucleotide variant (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722729	NM_001360016.2(G6PD):c.121-4460del	G6PD	Deletion (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722728	NM_001360016.2(G6PD):c.473G>A (p.Cys158Tyr)	G6PD (C158Y +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722727	NM_001360016.2(G6PD):c.463C>G (p.His155Asp)	G6PD (H155D +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic/Likely pathogenic
Select item 1722726	NM_001360016.2(G6PD):c.[376A>G;463C>G]	G6PD (N126D +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722725	NM_001360016.2(G6PD):c.442G>A (p.Glu148Lys)	G6PD (E148K +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722724	NM_001360016.2(G6PD):c.409C>T (p.Leu137Phe)	G6PD (L137F +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency +1 more	GLikely pathogenic
Select item 1722723	NM_001360016.2(G6PD):c.[375G>T;379G>T383T>C384C>T]	G6PD (L128P +5 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722722	NM_001360016.2(G6PD):c.120+3126T>C	G6PD, IKBKG +1 more	Single nucleotide variant (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722721	NM_001360016.2(G6PD):c.371A>G (p.His124Arg)	G6PD (H124R +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722720	NM_001360016.2(G6PD):c.356A>C (p.Gln119Pro)	G6PD (Q119P +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722719	NM_001360016.2(G6PD):c.352T>C (p.Tyr118His)	G6PD (Y118H +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722718	NM_001360016.2(G6PD):c.312C>T (p.Arg104=)	G6PD	Single nucleotide variant (synonymous variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722717	NM_001360016.2(G6PD):c.290A>T (p.Lys97Met)	G6PD (K127M +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722716	NM_001360016.2(G6PD):c.274C>T (p.Pro92Ser)	G6PD (P122S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722715	NM_001360016.2(G6PD):c.227C>A (p.Thr76Lys)	G6PD (T106K +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency +1 more	GConflicting classifications of pathogenicity
Select item 1722714	NM_001360016.2(G6PD):c.224T>C (p.Leu75Pro)	G6PD (L105P +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722713	NM_001360016.2(G6PD):c.120+2955A>G	G6PD, IKBKG +1 more	Single nucleotide variant (intron variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GBenign
Select item 1722712	NM_001360016.2(G6PD):c.219C>T (p.Ser73=)	G6PD	Single nucleotide variant (synonymous variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722711	NM_001360016.2(G6PD):c.[143T>C;202G>A]	G6PD (I48T +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722710	NM_001360016.2(G6PD):c.197T>G (p.Phe66Cys)	G6PD (F66C +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722709	NM_001360016.2(G6PD):c.187G>A (p.Glu63Lys)	G6PD (E63K +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722708	NM_001360016.2(G6PD):c.185C>T (p.Pro62Leu)	G6PD (P62L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722707	NM_001360016.2(G6PD):c.185C>A (p.Pro62His)	G6PD (P62H +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722706	NM_001360016.2(G6PD):c.179T>C (p.Leu60Pro)	G6PD (L60P +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722705	NM_001360016.2(G6PD):c.170G>A (p.Arg57Gln)	G6PD (R57Q +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722704	NM_001360016.2(G6PD):c.148C>T (p.Pro50Ser)	G6PD (P50S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency +1 more	GConflicting classifications of pathogenicity
Select item 1722703	NM_001360016.2(G6PD):c.988C>T (p.Arg330Cys)	G6PD (R330C +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency +1 more	GUncertain significance
Select item 1722702	NM_001360016.2(G6PD):c.*357G>A	G6PD	Single nucleotide variant (3 prime UTR variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722701	NM_001360016.2(G6PD):c.989G>A (p.Arg330His)	G6PD (R330H +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722700	NM_001360016.2(G6PD):c.701T>C (p.Ile234Thr)	G6PD (I234T +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722699	NM_001360016.2(G6PD):c.595A>G (p.Ile199Val)	G6PD (I199V +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GConflicting classifications of pathogenicity
Select item 1722698	NM_001360016.2(G6PD):c.[376A>G;563C>T]	G6PD (N126D +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722697	NM_001360016.2(G6PD):c.[202G>A;376A>G563C>T]	G6PD (V68M +5 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722696	NM_001360016.2(G6PD):c.[202G>A;563C>T]	G6PD (V68M +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722695	NM_001360016.2(G6PD):c.499A>T (p.Ile167Phe)	G6PD (I167F +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722694	NM_001360016.2(G6PD):c.472T>G (p.Cys158Gly)	G6PD (C158G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722693	NM_001360016.2(G6PD):c.[311G>A;376A>G]	G6PD (N126D +3 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722692	NM_001360016.2(G6PD):c.94C>G (p.His32Asp)	G6PD, IKBKG (H32D +1 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722691	NM_001360016.2(G6PD):c.197T>A (p.Phe66Tyr)	G6PD (F66Y +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722690	NM_001360016.2(G6PD):c.25C>T (p.Arg9Trp)	G6PD, IKBKG (R39W +1 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GUncertain significance
Select item 1722689	NM_001360016.2(G6PD):c.1466C>T (p.Pro489Leu)	G6PD (P489L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722688	NM_001360016.2(G6PD):c.1463G>T (p.Gly488Val)	G6PD (G488V +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722687	NM_001360016.2(G6PD):c.34G>T (p.Val12Leu)	G6PD, IKBKG (V12L +1 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722686	NM_001360016.2(G6PD):c.1292T>G (p.Val431Gly)	G6PD (V431G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722685	NM_001360016.2(G6PD):c.1288-2A>T	G6PD	Single nucleotide variant (splice acceptor variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722684	NM_001360016.2(G6PD):c.1285A>G (p.Lys429Glu)	G6PD (K429E +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722683	NM_001360016.2(G6PD):c.7G>A (p.Glu3Lys)	G6PD, IKBKG (E33K +1 more)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722682	NM_001360016.2(G6PD):c.1284C>A (p.Tyr428Ter)	G6PD (Y428* +1 more)	Single nucleotide variant (nonsense)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722681	NM_001360016.2(G6PD):c.1246G>A (p.Glu416Lys)	G6PD (E416K +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722680	NM_001360016.2(G6PD):c.1226C>G (p.Pro409Arg)	G6PD (P409R +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722679	NM_001360016.2(G6PD):c.1226C>A (p.Pro409Gln)	G6PD (P409Q +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722678	NM_001360016.2(G6PD):c.1225C>T (p.Pro409Ser)	G6PD (P409S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722677	NM_001360016.2(G6PD):c.1220A>C (p.Lys407Thr)	G6PD (K407T +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722676	NM_001360016.2(G6PD):c.1215G>A (p.Met405Ile)	G6PD (M405I +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722675	NM_001360016.2(G6PD):c.1205C>A (p.Thr402Asn)	G6PD (T402N +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722674	NM_000402.4(G6PD):c.7C>T (p.Arg3Trp)	G6PD, IKBKG +2 more (R3W)	Single nucleotide variant (missense variant +1 more)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely pathogenic
Select item 1722673	NM_001360016.2(G6PD):c.1183C>T (p.Gln395Ter)	G6PD (Q395* +1 more)	Single nucleotide variant (nonsense)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722672	NM_001360016.2(G6PD):c.1177C>G (p.Arg393Gly)	G6PD (R393G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722671	NM_001360016.2(G6PD):c.1155C>G (p.Cys385Trp)	G6PD (C385W +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722670	NM_001360016.2(G6PD):c.1153T>G (p.Cys385Gly)	G6PD (C385G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722669	NM_001360016.2(G6PD):c.1139T>C (p.Ile380Thr)	G6PD (I380T +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722668	NM_001360016.2(G6PD):c.1138A>G (p.Ile380Val)	G6PD (I380V +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722667	NM_001360016.2(G6PD):c.1118T>C (p.Phe373Ser)	G6PD (F373S +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722666	NM_001360016.2(G6PD):c.*272G>A	G6PD	Single nucleotide variant (3 prime UTR variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GLikely benign
Select item 1722665	NM_001360016.2(G6PD):c.997ACC[1] (p.Thr334del)	G6PD (T334del +1 more)	Microsatellite (inframe_deletion)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722664	NM_001360016.2(G6PD):c.848A>G (p.Asp283Gly)	G6PD (D283G +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722663	NM_001360016.2(G6PD):c.827C>T (p.Pro276Leu)	G6PD (P276L +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic
Select item 1722662	NM_001360016.2(G6PD):c.770G>A (p.Arg257Gln)	G6PD (R257Q +1 more)	Single nucleotide variant (missense variant)	Anemia, nonspherocytic hemolytic, due to G6PD deficiency	GPathogenic

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