"DNHD1-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 770398	NM_144666.3(DNHD1):c.9G>A (p.Pro3=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 782867	NM_144666.3(DNHD1):c.70C>A (p.His24Asn)	DNHD1 (H24N)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GLikely benign
Select item 788110	NM_144666.3(DNHD1):c.116A>G (p.Gln39Arg)	DNHD1 (Q39R)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 3059428	NM_144666.3(DNHD1):c.197G>A (p.Arg66Gln)	DNHD1 (R66Q)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3060797	NM_144666.3(DNHD1):c.570G>T (p.Leu190=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 3059265	NM_144666.3(DNHD1):c.719T>A (p.Val240Glu)	DNHD1 (V240E)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3057035	NM_144666.3(DNHD1):c.836A>C (p.Gln279Pro)	DNHD1 (Q279P)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 773243	NM_144666.3(DNHD1):c.898G>A (p.Val300Met)	DNHD1 (V300M)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GLikely benign
Select item 3055243	NM_144666.3(DNHD1):c.921-4A>G	DNHD1	Single nucleotide variant (intron variant)	DNHD1-related disorder	GBenign
Select item 3055372	NM_144666.3(DNHD1):c.949G>A (p.Asp317Asn)	DNHD1 (D317N)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 736881	NM_144666.3(DNHD1):c.950A>G (p.Asp317Gly)	DNHD1 (D317G)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 789480	NM_144666.3(DNHD1):c.1086A>G (p.Pro362=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3060931	NM_144666.3(DNHD1):c.1089C>T (p.Phe363=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 760706	NM_144666.3(DNHD1):c.1125T>C (p.Cys375=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GLikely benign
Select item 789038	NM_144666.3(DNHD1):c.1134G>C (p.Lys378Asn)	DNHD1 (K378N)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 736151	NM_144666.3(DNHD1):c.1160G>A (p.Arg387Gln)	DNHD1 (R387Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1272652	NM_144666.3(DNHD1):c.1252C>T (p.His418Tyr)	DNHD1 (H418Y)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 719539	NM_144666.3(DNHD1):c.1323C>T (p.Ala441=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign
Select item 776566	NM_144666.3(DNHD1):c.1392+9C>G	DNHD1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 776567	NM_144666.3(DNHD1):c.1482C>T (p.Tyr494=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3057048	NM_144666.3(DNHD1):c.1678C>G (p.Gln560Glu)	DNHD1 (Q560E)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3038342	NM_144666.3(DNHD1):c.1758A>G (p.Leu586=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 3039310	NM_144666.3(DNHD1):c.1785+17A>G	DNHD1	Single nucleotide variant (3 prime UTR variant +1 more)	DNHD1-related disorder	GLikely benign
Select item 1183642	NM_144666.3(DNHD1):c.1865A>C (p.Asp622Ala)	DNHD1 (D622A)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3044163	NM_144666.3(DNHD1):c.1969G>T (p.Ala657Ser)	DNHD1 (A657S)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GUncertain significance
Select item 1287986	NM_144666.3(DNHD1):c.2081A>G (p.Asn694Ser)	DNHD1 (N694S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1283833	NM_144666.3(DNHD1):c.2090A>G (p.Gln697Arg)	DNHD1 (Q697R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3041343	NM_144666.3(DNHD1):c.2215C>A (p.Pro739Thr)	DNHD1 (P739T)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 674309	NM_144666.3(DNHD1):c.2305G>A (p.Gly769Arg)	DNHD1 (G769R)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3048010	NM_144666.3(DNHD1):c.2394A>G (p.Gln798=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 3044653	NM_144666.3(DNHD1):c.2535G>A (p.Glu845=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 1244174	NM_144666.3(DNHD1):c.2536C>A (p.Leu846Met)	DNHD1 (L846M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 717169	NM_144666.3(DNHD1):c.2561G>A (p.Arg854Gln)	DNHD1 (R854Q)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3037444	NM_144666.3(DNHD1):c.2646C>T (p.Phe882=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 806605	NM_144666.3(DNHD1):c.2683C>T (p.Gln895Ter)	DNHD1 (Q895*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 774620	NM_144666.3(DNHD1):c.2839G>T (p.Glu947Ter)	DNHD1 (E947*)	Single nucleotide variant (nonsense)	Spermatogenic failure 65 +2 more	GBenign/Likely benign
Select item 3045675	NM_144666.3(DNHD1):c.2911G>A (p.Glu971Lys)	DNHD1 (E971K)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GUncertain significance
Select item 3049756	NM_144666.3(DNHD1):c.2936G>A (p.Arg979His)	DNHD1 (R979H)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3042736	NM_144666.3(DNHD1):c.2958C>T (p.Ser986=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 3053322	NM_144666.3(DNHD1):c.3028T>C (p.Cys1010Arg)	DNHD1 (C1010R)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3038633	NM_144666.3(DNHD1):c.3087C>T (p.Ser1029=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 774688	NM_144666.3(DNHD1):c.3246G>A (p.Glu1082=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 3038951	NM_144666.3(DNHD1):c.3450T>C (p.His1150=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 3058882	NM_144666.3(DNHD1):c.3585A>G (p.Gln1195=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 682604	NM_144666.3(DNHD1):c.3612C>T (p.Gly1204=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3033501	NM_144666.3(DNHD1):c.3633C>T (p.Tyr1211=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 715738	NM_144666.3(DNHD1):c.3736G>A (p.Ala1246Thr)	DNHD1 (A1246T)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 727475	NM_144666.3(DNHD1):c.4041C>T (p.Ser1347=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 742167	NM_144666.3(DNHD1):c.4060G>A (p.Ala1354Thr)	DNHD1 (A1354T)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 722069	NM_144666.3(DNHD1):c.4072C>T (p.Arg1358Cys)	DNHD1 (R1358C)	Single nucleotide variant (missense variant)	DNHD1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 718552	NM_144666.3(DNHD1):c.4080C>G (p.Phe1360Leu)	DNHD1 (F1360L)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 726521	NM_144666.3(DNHD1):c.4908G>A (p.Ala1636=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign
Select item 3056402	NM_144666.3(DNHD1):c.4927C>T (p.Leu1643=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 770969	NM_144666.3(DNHD1):c.5264G>A (p.Arg1755His)	DNHD1 (R1755H)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 3045979	NM_144666.3(DNHD1):c.5419C>T (p.Leu1807=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 3055808	NM_144666.3(DNHD1):c.5422C>T (p.Arg1808Cys)	DNHD1 (R1808C)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 829807	NM_144666.3(DNHD1):c.5617C>A (p.Arg1873Ser)	DNHD1 (R1873S)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 786586	NM_144666.3(DNHD1):c.5657G>A (p.Arg1886Gln)	DNHD1 (R1886Q)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3038060	NM_144666.3(DNHD1):c.5688G>C (p.Lys1896Asn)	DNHD1 (K1896N)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3051131	NM_144666.3(DNHD1):c.5737_5738insAT (p.Arg1913fs)	DNHD1 (R1913fs)	Insertion (frameshift variant)	DNHD1-related disorder	GLikely benign
Select item 774323	NM_144666.3(DNHD1):c.5793G>A (p.Leu1931=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 728699	NM_144666.3(DNHD1):c.5904C>T (p.Ser1968=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 3060722	NM_144666.3(DNHD1):c.6044T>C (p.Met2015Thr)	DNHD1 (M2015T)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 770970	NM_144666.3(DNHD1):c.6064G>C (p.Gly2022Arg)	DNHD1 (G2022R)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 3038148	NM_144666.3(DNHD1):c.6121T>C (p.Phe2041Leu)	DNHD1 (F2041L)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 780945	NM_144666.3(DNHD1):c.6186C>T (p.Ala2062=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3041231	NM_144666.3(DNHD1):c.6498T>C (p.Tyr2166=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 773652	NM_144666.3(DNHD1):c.6618G>A (p.Gly2206=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 709450	NM_144666.3(DNHD1):c.6624G>A (p.Gln2208=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 776568	NM_144666.3(DNHD1):c.6664C>T (p.Arg2222Cys)	DNHD1 (R2222C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1678807	NM_144666.3(DNHD1):c.6697C>T (p.Arg2233Cys)	DNHD1 (R2233C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2224707	NM_144666.3(DNHD1):c.7056C>G (p.Ser2352Arg)	DNHD1 (S2352R)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1183802	NM_144666.3(DNHD1):c.7120G>A (p.Val2374Met)	DNHD1 (V2374M)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 786587	NM_144666.3(DNHD1):c.7295G>A (p.Gly2432Asp)	DNHD1 (G2432D)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3038805	NM_144666.3(DNHD1):c.7388-3T>C	DNHD1	Single nucleotide variant (intron variant)	DNHD1-related disorder	GLikely benign
Select item 3056760	NM_144666.3(DNHD1):c.7479G>A (p.Thr2493=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 790457	NM_144666.3(DNHD1):c.7575G>A (p.Leu2525=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign/Likely benign
Select item 779134	NM_144666.3(DNHD1):c.7623T>C (p.Pro2541=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 789481	NM_144666.3(DNHD1):c.7646G>A (p.Arg2549His)	DNHD1 (R2549H)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 790361	NM_144666.3(DNHD1):c.7818C>T (p.Asn2606=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GLikely benign
Select item 770399	NM_144666.3(DNHD1):c.8116C>A (p.Pro2706Thr)	DNHD1 (P2706T)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2636090	NM_144666.3(DNHD1):c.8119G>A (p.Glu2707Lys)	DNHD1 (E2707K)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GUncertain significance
Select item 3050345	NM_144666.3(DNHD1):c.8184G>A (p.Glu2728=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 3056370	NM_144666.3(DNHD1):c.8263C>T (p.Pro2755Ser)	DNHD1 (P2755S)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3037263	NM_144666.3(DNHD1):c.8267T>C (p.Val2756Ala)	DNHD1 (V2756A)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3051882	NM_144666.3(DNHD1):c.8328A>G (p.Ala2776=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 3059219	NM_144666.3(DNHD1):c.8581C>A (p.His2861Asn)	DNHD1 (H2861N)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3055943	NM_144666.3(DNHD1):c.8581C>T (p.His2861Tyr)	DNHD1 (H2861Y)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GBenign
Select item 3055834	NM_144666.3(DNHD1):c.8829G>C (p.Leu2943=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 3053434	NM_144666.3(DNHD1):c.8859A>C (p.Thr2953=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GLikely benign
Select item 724237	NM_144666.3(DNHD1):c.8960T>C (p.Leu2987Pro)	DNHD1 (L2987P)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 724238	NM_144666.3(DNHD1):c.9122T>C (p.Ile3041Thr)	DNHD1 (I3041T)	Single nucleotide variant (missense variant)	DNHD1-related disorder +1 more	GBenign
Select item 3051537	NM_144666.3(DNHD1):c.9211G>A (p.Gly3071Ser)	DNHD1 (G3071S)	Single nucleotide variant (missense variant)	DNHD1-related disorder	GLikely benign
Select item 785338	NM_144666.3(DNHD1):c.9463G>A (p.Gly3155Ser)	DNHD1 (G3155S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3056797	NM_144666.3(DNHD1):c.9501G>A (p.Gln3167=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder	GBenign
Select item 707873	NM_144666.3(DNHD1):c.9598G>C (p.Glu3200Gln)	DNHD1 (E3200Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 724239	NM_144666.3(DNHD1):c.9639G>A (p.Leu3213=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GBenign
Select item 3046816	NM_144666.3(DNHD1):c.9669+3G>A	DNHD1	Single nucleotide variant (intron variant)	DNHD1-related disorder	GLikely benign
Select item 718338	NM_144666.3(DNHD1):c.9792C>T (p.Phe3264=)	DNHD1	Single nucleotide variant (synonymous variant)	DNHD1-related disorder +1 more	GLikely benign
Select item 2641553	NM_144666.3(DNHD1):c.9804A>G (p.Thr3268=)	DNHD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

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