"TEX15-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 770379	NM_001350162.2(TEX15):c.9368C>T (p.Ser3123Phe)	TEX15 (S3123F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3040229	NM_001350162.2(TEX15):c.8860C>G (p.Leu2954Val)	TEX15 (L2571V +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GBenign
Select item 771877	NM_001350162.2(TEX15):c.8622C>A (p.Ser2874=)	TEX15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3035454	NM_001350162.2(TEX15):c.8331A>C (p.Leu2777=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 3046249	NM_001350162.2(TEX15):c.8222+8T>C	TEX15	Single nucleotide variant (intron variant)	TEX15-related disorder	GBenign
Select item 3041514	NM_001350162.2(TEX15):c.7540G>A (p.Ala2514Thr)	TEX15 (A2131T +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GLikely benign
Select item 733695	NM_001350162.2(TEX15):c.7244A>G (p.Asn2415Ser)	TEX15 (N2415S)	Single nucleotide variant (missense variant)	TEX15-related disorder +1 more	GLikely benign
Select item 3056782	NM_001350162.2(TEX15):c.7085A>G (p.Asn2362Ser)	TEX15 (N1979S +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GBenign
Select item 783521	NM_001350162.2(TEX15):c.7045G>A (p.Glu2349Lys)	TEX15 (E2349K)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3048833	NM_001350162.2(TEX15):c.6909G>A (p.Val2303=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 3047476	NM_001350162.2(TEX15):c.6696A>G (p.Pro2232=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 776312	NM_001350162.2(TEX15):c.6552C>T (p.Ser2184=)	TEX15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3057695	NM_001350162.2(TEX15):c.6117A>G (p.Glu2039=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 3043376	NM_001350162.2(TEX15):c.5857C>G (p.Leu1953Val)	TEX15 (L1570V +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GLikely benign
Select item 3056196	NM_001350162.2(TEX15):c.5688T>G (p.Asp1896Glu)	TEX15 (D1513E +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GBenign
Select item 1176880	NM_001350162.2(TEX15):c.4944C>G (p.Asp1648Glu)	TEX15 (D1648E)	Single nucleotide variant (missense variant)	Spermatogenic failure 25 +2 more	GBenign/Likely benign
Select item 3060643	NM_001350162.2(TEX15):c.4692T>C (p.Asp1564=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GBenign
Select item 784127	NM_001350162.2(TEX15):c.4665A>G (p.Ala1555=)	TEX15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3048795	NM_001350162.2(TEX15):c.4569C>T (p.Ser1523=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 3034144	NM_001350162.2(TEX15):c.4188A>G (p.Thr1396=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GLikely benign
Select item 789764	NM_001350162.2(TEX15):c.3959G>A (p.Arg1320Gln)	TEX15 (R1320Q)	Single nucleotide variant (missense variant)	TEX15-related disorder +1 more	GBenign
Select item 708791	NM_001350162.2(TEX15):c.3563C>T (p.Ala1188Val)	TEX15 (A1188V)	Single nucleotide variant (missense variant)	TEX15-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 730576	NM_001350162.2(TEX15):c.3510G>A (p.Pro1170=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder +1 more	GBenign/Likely benign
Select item 3035949	NM_001350162.2(TEX15):c.3509C>T (p.Pro1170Leu)	TEX15 (P1170L +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GLikely benign
Select item 3039857	NM_001350162.2(TEX15):c.3485A>G (p.Asn1162Ser)	TEX15 (N1162S +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GBenign
Select item 3036434	NM_001350162.2(TEX15):c.3164T>C (p.Ile1055Thr)	TEX15 (I1055T +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GLikely benign
Select item 3050625	NM_001350162.2(TEX15):c.2515C>T (p.Leu839=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related disorder	GBenign
Select item 3034615	NM_001350162.2(TEX15):c.1868A>G (p.Asn623Ser)	TEX15 (N240S +1 more)	Single nucleotide variant (missense variant)	TEX15-related disorder	GLikely benign
Select item 789765	NM_001350162.2(TEX15):c.1350A>T (p.Ala450=)	TEX15	Single nucleotide variant (synonymous variant +1 more)	TEX15-related disorder +1 more	GBenign
Select item 2658524	NM_001350162.2(TEX15):c.993G>A (p.Glu331=)	TEX15	Single nucleotide variant (synonymous variant +1 more)	TEX15-related disorder +1 more	GLikely benign
Select item 3040149	NM_001350162.2(TEX15):c.614A>C (p.Asn205Thr)	TEX15 (N205T)	Single nucleotide variant (missense variant +1 more)	TEX15-related disorder	GLikely benign
Select item 3040591	NM_001350162.2(TEX15):c.541-4_541-3dup	TEX15	Duplication (intron variant)	TEX15-related disorder	GLikely benign
Select item 3060166	NM_001350162.2(TEX15):c.261G>T (p.Leu87=)	TEX15	Single nucleotide variant (synonymous variant +1 more)	TEX15-related disorder	GBenign

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Items: 33