TASOR2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155636	GRCh38/hg38 10p15.3-12.31(chr10:54086-19336980)x1	PROSER2-AS1, PRPF18 +680 more	Copy number loss	See cases	GPathogenic
Select item 154187	GRCh38/hg38 10p15.3-13(chr10:54086-13205916)x3	MIR5699, MIR6072 +496 more	Copy number gain	See cases	GPathogenic
Select item 58710	GRCh38/hg38 10p15.3-15.1(chr10:69260-6209368)x1	ADARB2, ADARB2-AS1 +276 more	Copy number loss	See cases	GPathogenic
Select item 59657	GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	LOC126860819, LOC126860820 +680 more	Copy number gain	See cases	GPathogenic
Select item 150048	GRCh38/hg38 10p15.3-13(chr10:70478-13736564)x1	LOC130003277, LOC130003278 +520 more	Copy number loss	See cases	GPathogenic
Select item 146014	GRCh38/hg38 10p15.3-13(chr10:73856-12815915)x3	LOC132090805, MANCR +482 more	Copy number gain	See cases	GPathogenic
Select item 149407	GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	ACBD7, ACBD7-DCLRE1CP1 +837 more	Copy number gain	See cases	GPathogenic
Select item 146220	GRCh38/hg38 10p15.3-14(chr10:90421-11713049)x3	LOC130003153, LOC130003154 +421 more	Copy number gain	See cases	GPathogenic
Select item 57431	GRCh38/hg38 10p15.3-14(chr10:90421-6769994)x3	ADARB2, ADARB2-AS1 +298 more	Copy number gain	See cases	GPathogenic
Select item 57407	GRCh38/hg38 10p15.3-14(chr10:90421-8442783)x3	ADARB2, ADARB2-AS1 +352 more	Copy number gain	See cases	GPathogenic
Select item 154099	GRCh38/hg38 10p15.3-14(chr10:1601172-9203729)x3	ADARB2, AKR1C1 +304 more	Copy number gain	See cases	GLikely pathogenic
Select item 545134	Single allele	LOC130003188, LOC130003189 +195 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 146553	GRCh38/hg38 10p15.1-14(chr10:4605831-7403265)x1	AKR1C1, AKR1C2 +175 more	Copy number loss	See cases	GUncertain significance
Select item 58717	GRCh38/hg38 10p15.1-13(chr10:4802753-16823491)x1	LOC130003217, LOC130003218 +482 more	Copy number loss	See cases	GPathogenic
Select item 148178	GRCh38/hg38 10p15.1(chr10:4871826-5811361)x3	AKR1C1, AKR1C2 +52 more	Copy number gain	See cases	GUncertain significance
Select item 3174269	NM_001321783.2(TASOR2):c.50T>G (p.Leu17Arg)	TASOR2 (L17R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174272	NM_001321783.2(TASOR2):c.52A>G (p.Met18Val)	TASOR2 (M18V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613293	NM_001321783.2(TASOR2):c.66A>C (p.Lys22Asn)	TASOR2 (K22N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174199	NM_001321783.2(TASOR2):c.106G>A (p.Ala36Thr)	TASOR2 (A251T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174209	NM_001321783.2(TASOR2):c.124G>A (p.Gly42Ser)	TASOR2 (G257S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174216	NM_001321783.2(TASOR2):c.177G>T (p.Met59Ile)	TASOR2 (M59I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324520	NM_001321783.2(TASOR2):c.295A>G (p.Asn99Asp)	TASOR2 (N314D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535963	NM_001321783.2(TASOR2):c.374A>G (p.Asp125Gly)	TASOR2 (D125G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174245	NM_001321783.2(TASOR2):c.377G>A (p.Arg126Gln)	TASOR2 (R126Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174255	NM_001321783.2(TASOR2):c.434G>T (p.Gly145Val)	TASOR2 (G360V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174258	NM_001321783.2(TASOR2):c.444G>T (p.Met148Ile)	TASOR2 (M148I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174262	NM_001321783.2(TASOR2):c.479T>C (p.Leu160Pro)	TASOR2 (L375P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174267	NM_001321783.2(TASOR2):c.499T>A (p.Leu167Met)	TASOR2 (L382M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523790	NM_001321783.2(TASOR2):c.554A>G (p.Asn185Ser)	TASOR2 (N400S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174289	NM_001321783.2(TASOR2):c.605C>A (p.Pro202Gln)	TASOR2 (P202Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174290	NM_001321783.2(TASOR2):c.623G>A (p.Arg208His)	TASOR2 (R208H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2545450	NM_001321783.2(TASOR2):c.643A>G (p.Lys215Glu)	TASOR2 (K430E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463242	NM_001321783.2(TASOR2):c.647C>T (p.Ala216Val)	TASOR2 (A431V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174300	NM_001321783.2(TASOR2):c.710G>A (p.Gly237Glu)	TASOR2 (G237E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174301	NM_001321783.2(TASOR2):c.740C>G (p.Pro247Arg)	TASOR2 (P462R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482085	NM_001321783.2(TASOR2):c.743C>T (p.Pro248Leu)	TASOR2 (P248L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596607	NM_001321783.2(TASOR2):c.751A>G (p.Lys251Glu)	TASOR2 (K251E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324527	NM_001321783.2(TASOR2):c.770T>C (p.Leu257Ser)	TASOR2 (L257S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531441	NM_001321783.2(TASOR2):c.817G>A (p.Glu273Lys)	TASOR2 (E273K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324524	NM_001321783.2(TASOR2):c.860C>G (p.Ser287Cys)	TASOR2 (S287C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324539	NM_001321783.2(TASOR2):c.928C>T (p.Leu310Phe)	TASOR2 (L525F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174302	NM_001321783.2(TASOR2):c.946G>A (p.Val316Met)	TASOR2 (V531M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174303	NM_001321783.2(TASOR2):c.950G>A (p.Arg317Lys)	TASOR2 (R317K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174197	NM_001321783.2(TASOR2):c.1050G>T (p.Lys350Asn)	TASOR2 (K565N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174198	NM_001321783.2(TASOR2):c.1053G>C (p.Arg351Ser)	TASOR2 (R351S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456974	NM_001321783.2(TASOR2):c.1064T>C (p.Met355Thr)	TASOR2 (M355T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174200	NM_001321783.2(TASOR2):c.1073T>C (p.Met358Thr)	TASOR2 (M573T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174201	NM_001321783.2(TASOR2):c.1084A>G (p.Lys362Glu)	TASOR2 (K362E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174202	NM_001321783.2(TASOR2):c.1102C>T (p.Arg368Cys)	TASOR2 (R368C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174203	NM_001321783.2(TASOR2):c.1103G>A (p.Arg368His)	TASOR2 (R368H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174204	NM_001321783.2(TASOR2):c.1105C>G (p.Pro369Ala)	TASOR2 (P584A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174205	NM_001321783.2(TASOR2):c.1112C>T (p.Pro371Leu)	TASOR2 (P371L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174206	NM_001321783.2(TASOR2):c.1129A>G (p.Arg377Gly)	TASOR2 (R592G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174207	NM_001321783.2(TASOR2):c.1141A>G (p.Ser381Gly)	TASOR2 (S596G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174208	NM_001321783.2(TASOR2):c.1227G>T (p.Gln409His)	TASOR2 (Q409H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174210	NM_001321783.2(TASOR2):c.1273A>T (p.Ile425Phe)	TASOR2 (I640F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589501	NM_001321783.2(TASOR2):c.1348C>G (p.Pro450Ala)	TASOR2 (P450A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174211	NM_001321783.2(TASOR2):c.1420C>T (p.Pro474Ser)	TASOR2 (P689S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521031	NM_001321783.2(TASOR2):c.1559A>G (p.Asp520Gly)	TASOR2 (D735G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174212	NM_001321783.2(TASOR2):c.1579G>A (p.Val527Ile)	TASOR2 (V446I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174213	NM_001321783.2(TASOR2):c.1615G>A (p.Asp539Asn)	TASOR2 (D539N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324540	NM_001321783.2(TASOR2):c.1679C>T (p.Ser560Phe)	TASOR2 (S479F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174214	NM_001321783.2(TASOR2):c.1691C>T (p.Pro564Leu)	TASOR2 (P564L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472357	NM_001321783.2(TASOR2):c.1712C>G (p.Ser571Cys)	TASOR2 (S490C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174215	NM_001321783.2(TASOR2):c.1760G>A (p.Gly587Glu)	TASOR2 (G587E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324521	NM_001321783.2(TASOR2):c.1907A>G (p.Glu636Gly)	TASOR2 (E636G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324538	NM_001321783.2(TASOR2):c.1943C>A (p.Ser648Tyr)	TASOR2 (S567Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174217	NM_001321783.2(TASOR2):c.1982C>T (p.Thr661Ile)	TASOR2 (T580I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324529	NM_001321783.2(TASOR2):c.1995G>T (p.Lys665Asn)	TASOR2 (K584N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174218	NM_001321783.2(TASOR2):c.1997A>G (p.Lys666Arg)	TASOR2 (K666R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174219	NM_001321783.2(TASOR2):c.2107G>A (p.Gly703Ser)	TASOR2 (G622S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174220	NM_001321783.2(TASOR2):c.2131C>A (p.Pro711Thr)	TASOR2 (P630T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324517	NM_001321783.2(TASOR2):c.2143G>A (p.Val715Met)	TASOR2 (V715M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2590521	NM_001321783.2(TASOR2):c.2191T>C (p.Ser731Pro)	TASOR2 (S946P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545753	NM_001321783.2(TASOR2):c.2201G>A (p.Arg734His)	TASOR2 (R653H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174221	NM_001321783.2(TASOR2):c.2256A>C (p.Glu752Asp)	TASOR2 (E671D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532464	NM_001321783.2(TASOR2):c.2288A>G (p.Asn763Ser)	TASOR2 (N763S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531968	NM_001321783.2(TASOR2):c.2362G>A (p.Glu788Lys)	TASOR2 (E1003K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324525	NM_001321783.2(TASOR2):c.2423T>G (p.Ile808Arg)	TASOR2 (I1023R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174222	NM_001321783.2(TASOR2):c.2453G>A (p.Ser818Asn)	TASOR2 (S1033N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174223	NM_001321783.2(TASOR2):c.2454C>A (p.Ser818Arg)	TASOR2 (S1033R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324516	NM_001321783.2(TASOR2):c.2507G>A (p.Arg836His)	TASOR2 (R836H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570454	NM_001321783.2(TASOR2):c.2513T>A (p.Ile838Asn)	TASOR2 (I838N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621358	NM_001321783.2(TASOR2):c.2594A>G (p.Glu865Gly)	TASOR2 (E865G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518768	NM_001321783.2(TASOR2):c.2606G>A (p.Arg869His)	TASOR2 (R788H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174224	NM_001321783.2(TASOR2):c.2618G>A (p.Cys873Tyr)	TASOR2 (C792Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174225	NM_001321783.2(TASOR2):c.2662C>A (p.Leu888Ile)	TASOR2 (L1103I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174226	NM_001321783.2(TASOR2):c.2694T>G (p.Phe898Leu)	TASOR2 (F1113L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601233	NM_001321783.2(TASOR2):c.2816G>A (p.Gly939Asp)	TASOR2 (G1154D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174228	NM_001321783.2(TASOR2):c.2849T>C (p.Val950Ala)	TASOR2 (V1165A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324528	NM_001321783.2(TASOR2):c.2861A>G (p.Glu954Gly)	TASOR2 (E1169G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174229	NM_001321783.2(TASOR2):c.2881G>A (p.Asp961Asn)	TASOR2 (D880N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470392	NM_001321783.2(TASOR2):c.3040A>G (p.Thr1014Ala)	TASOR2 (T1229A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541579	NM_001321783.2(TASOR2):c.3061A>G (p.Ile1021Val)	TASOR2 (I1236V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174230	NM_001321783.2(TASOR2):c.3146C>T (p.Pro1049Leu)	TASOR2 (P1049L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174231	NM_001321783.2(TASOR2):c.3181C>T (p.His1061Tyr)	TASOR2 (H1276Y +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3174232	NM_001321783.2(TASOR2):c.3199G>C (p.Glu1067Gln)	TASOR2 (E1067Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174233	NM_001321783.2(TASOR2):c.3232T>C (p.Phe1078Leu)	TASOR2 (F1293L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604313	NM_001321783.2(TASOR2):c.3236A>G (p.Lys1079Arg)	TASOR2 (K998R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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