"Invitae"[submitter] AND "TEX15"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 753542	NM_001350162.2(TEX15):c.9474G>A (p.Trp3158Ter)	TEX15 (W3158*)	Single nucleotide variant (nonsense)	not provided	GConflicting classifications of pathogenicity
Select item 788821	NM_001350162.2(TEX15):c.9462A>G (p.Pro3154=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 770379	NM_001350162.2(TEX15):c.9368C>T (p.Ser3123Phe)	TEX15 (S3123F)	Single nucleotide variant (missense variant)	TEX15-related condition +1 more	GBenign
Select item 684768	NM_001350162.2(TEX15):c.9223G>A (p.Gly3075Arg)	TEX15 (G3075R)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 777420	NM_001350162.2(TEX15):c.8838T>G (p.Ile2946Met)	TEX15 (I2946M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
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 730699	NM_001350162.2(TEX15):c.7435T>G (p.Leu2479Val)	TEX15 (L2479V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 730700	NM_001350162.2(TEX15):c.7304T>C (p.Ile2435Thr)	TEX15 (I2435T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 712693	NM_001350162.2(TEX15):c.7297G>A (p.Glu2433Lys)	TEX15 (E2433K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 733695	NM_001350162.2(TEX15):c.7244A>G (p.Asn2415Ser)	TEX15 (N2415S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 783521	NM_001350162.2(TEX15):c.7045G>A (p.Glu2349Lys)	TEX15 (E2349K)	Single nucleotide variant (missense variant)	TEX15-related condition +1 more	GBenign/Likely benign
Select item 1071185	NM_001350162.2(TEX15):c.6906_6907del (p.Arg2302fs)	TEX15 (R2302fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
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 712695	NM_001350162.2(TEX15):c.5975A>G (p.Asn1992Ser)	TEX15 (N1992S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 776313	NM_001350162.2(TEX15):c.5465A>G (p.Lys1822Arg)	TEX15 (K1822R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712697	NM_001350162.2(TEX15):c.5296C>A (p.Leu1766Ile)	TEX15 (L1766I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712795	NM_001350162.2(TEX15):c.5103T>A (p.Leu1701=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712796	NM_001350162.2(TEX15):c.5067G>C (p.Glu1689Asp)	TEX15 (E1689D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712060	NM_001350162.2(TEX15):c.4945G>A (p.Val1649Ile)	TEX15 (V1649I)	Single nucleotide variant (missense variant)	Spermatogenic failure 25 +1 more	GConflicting classifications of pathogenicity
Select item 784127	NM_001350162.2(TEX15):c.4665A>G (p.Ala1555=)	TEX15	Single nucleotide variant (synonymous variant)	TEX15-related condition +1 more	GBenign/Likely benign
Select item 790605	NM_001350162.2(TEX15):c.4617C>T (p.Ser1539=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 722248	NM_001350162.2(TEX15):c.4185C>T (p.His1395=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2065070	NM_001350162.2(TEX15):c.4036C>T (p.Arg1346Ter)	TEX15 (R1346*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 789764	NM_001350162.2(TEX15):c.3959G>A (p.Arg1320Gln)	TEX15 (R1320Q)	Single nucleotide variant (missense variant)	TEX15-related condition +1 more	GBenign
Select item 708791	NM_001350162.2(TEX15):c.3563C>T (p.Ala1188Val)	TEX15 (A1188V)	Single nucleotide variant (missense variant)	Spermatogenic failure 25 +2 more	GConflicting classifications of pathogenicity
Select item 730576	NM_001350162.2(TEX15):c.3510G>A (p.Pro1170=)	TEX15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 712797	NM_001350162.2(TEX15):c.3319G>C (p.Ala1107Pro)	TEX15 (A1107P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 740926	NM_001350162.2(TEX15):c.3270G>T (p.Val1090=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 776314	NM_001350162.2(TEX15):c.2786A>G (p.Asp929Gly)	TEX15 (D929G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712798	NM_001350162.2(TEX15):c.2631C>T (p.Asn877=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 835432	NM_001350162.2(TEX15):c.2574_2581del (p.Thr859fs)	TEX15 (T859fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 786115	NM_001350162.2(TEX15):c.2434A>T (p.Asn812Tyr)	TEX15 (N812Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 712799	NM_001350162.2(TEX15):c.1978A>G (p.Ile660Val)	TEX15 (I660V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712800	NM_001350162.2(TEX15):c.1611T>C (p.Asn537=)	TEX15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 789765	NM_001350162.2(TEX15):c.1350A>T (p.Ala450=)	TEX15	Single nucleotide variant (synonymous variant +1 more)	TEX15-related condition +1 more	GBenign
Select item 768232	NM_001350162.2(TEX15):c.1197T>C (p.Asn399=)	TEX15	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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Items: 36