ASB2[gene] and "single gene"[properties] - ClinVar

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Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2591514	NM_001202429.2(ASB2):c.1835G>A (p.Arg612His)	ASB2 (R564H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334081	NM_001202429.2(ASB2):c.1835G>T (p.Arg612Leu)	ASB2 (R564L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130169	NM_001202429.2(ASB2):c.1834C>T (p.Arg612Cys)	ASB2 (R564C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555928	NM_001202429.2(ASB2):c.1826G>T (p.Gly609Val)	ASB2 (G609V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204975	NM_001202429.2(ASB2):c.1814G>A (p.Arg605Gln)	ASB2 (R557Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130168	NM_001202429.2(ASB2):c.1783C>A (p.Pro595Thr)	ASB2 (P595T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317542	NM_001202429.2(ASB2):c.1696A>G (p.Asn566Asp)	ASB2 (N518D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593468	NM_001202429.2(ASB2):c.1672G>A (p.Asp558Asn)	ASB2 (D510N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130167	NM_001202429.2(ASB2):c.1671C>G (p.Ile557Met)	ASB2 (I557M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496498	NM_001202429.2(ASB2):c.1666A>T (p.Ile556Phe)	ASB2 (I508F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603196	NM_001202429.2(ASB2):c.1589C>T (p.Ala530Val)	ASB2 (A530V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2338571	NM_001202429.2(ASB2):c.1589C>A (p.Ala530Glu)	ASB2 (A482E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130166	NM_001202429.2(ASB2):c.1577A>G (p.Asn526Ser)	ASB2 (N478S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3130165	NM_001202429.2(ASB2):c.1573T>G (p.Phe525Val)	ASB2 (F477V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317532	NM_001202429.2(ASB2):c.1561C>G (p.Pro521Ala)	ASB2 (P473A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535806	NM_001202429.2(ASB2):c.1541C>A (p.Pro514Gln)	ASB2 (P466Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317511	NM_001202429.2(ASB2):c.1537G>C (p.Gly513Arg)	ASB2 (G465R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317552	NM_001202429.2(ASB2):c.1505G>A (p.Gly502Asp)	ASB2 (G502D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317563	NM_001202429.2(ASB2):c.1457T>C (p.Met486Thr)	ASB2 (M438T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556520	NM_001202429.2(ASB2):c.1436C>A (p.Pro479His)	ASB2 (P431H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610735	NM_001202429.2(ASB2):c.1390G>A (p.Gly464Ser)	ASB2 (G416S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605047	NM_001202429.2(ASB2):c.1359C>G (p.Cys453Trp)	ASB2 (C453W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374202	NM_001202429.2(ASB2):c.1358G>A (p.Cys453Tyr)	ASB2 (C405Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130162	NM_001202429.2(ASB2):c.1291C>A (p.Leu431Met)	ASB2 (L431M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370619	NM_001202429.2(ASB2):c.1249T>C (p.Phe417Leu)	ASB2 (F417L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130161	NM_001202429.2(ASB2):c.1228C>T (p.Arg410Trp)	ASB2 (R410W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605289	NM_001202429.2(ASB2):c.1163T>A (p.Leu388Gln)	ASB2 (L340Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317494	NM_001202429.2(ASB2):c.1143C>G (p.His381Gln)	ASB2 (H333Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130160	NM_001202429.2(ASB2):c.1135C>A (p.Arg379Ser)	ASB2 (R379S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130159	NM_001202429.2(ASB2):c.1033T>C (p.Ser345Pro)	ASB2 (S297P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512080	NM_001202429.2(ASB2):c.1019C>T (p.Pro340Leu)	ASB2 (P292L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220112	NM_001202429.2(ASB2):c.1009G>A (p.Gly337Ser)	ASB2 (G289S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609480	NM_001202429.2(ASB2):c.993C>A (p.Asn331Lys)	ASB2 (N283K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473855	NM_001202429.2(ASB2):c.988G>A (p.Ala330Thr)	ASB2 (A282T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249528	NM_001202429.2(ASB2):c.913G>A (p.Ala305Thr)	ASB2 (A257T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317475	NM_001202429.2(ASB2):c.907G>A (p.Asp303Asn)	ASB2 (D255N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317522	NM_001202429.2(ASB2):c.898C>A (p.Gln300Lys)	ASB2 (Q252K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130176	NM_001202429.2(ASB2):c.845G>A (p.Gly282Glu)	ASB2 (G234E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558253	NM_001202429.2(ASB2):c.829G>C (p.Val277Leu)	ASB2 (V229L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565567	NM_001202429.2(ASB2):c.790G>C (p.Val264Leu)	ASB2 (V216L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522102	NM_001202429.2(ASB2):c.730G>A (p.Glu244Lys)	ASB2 (E196K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317505	NM_001202429.2(ASB2):c.709C>T (p.Arg237Cys)	ASB2 (R237C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130175	NM_001202429.2(ASB2):c.708C>A (p.Asn236Lys)	ASB2 (N188K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544029	NM_001202429.2(ASB2):c.685G>A (p.Ala229Thr)	ASB2 (A181T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400733	NM_001202429.2(ASB2):c.661G>A (p.Val221Met)	ASB2 (V173M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130174	NM_001202429.2(ASB2):c.644G>A (p.Arg215His)	ASB2 (R167H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252389	NM_001202429.2(ASB2):c.622C>T (p.Pro208Ser)	ASB2 (P160S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398468	NM_001202429.2(ASB2):c.591G>C (p.Glu197Asp)	ASB2 (E149D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323652	NM_001202429.2(ASB2):c.586G>A (p.Ala196Thr)	ASB2 (A148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130173	NM_001202429.2(ASB2):c.526G>A (p.Val176Ile)	ASB2 (V176I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130172	NM_001202429.2(ASB2):c.476G>A (p.Arg159Gln)	ASB2 (R111Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3130171	NM_001202429.2(ASB2):c.458G>A (p.Cys153Tyr)	ASB2 (C105Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305432	NM_001202429.2(ASB2):c.449A>G (p.Gln150Arg)	ASB2 (Q102R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317467	NM_001202429.2(ASB2):c.446G>A (p.Gly149Asp)	ASB2 (G149D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234622	NM_001202429.2(ASB2):c.394G>A (p.Ala132Thr)	ASB2 (A132T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206862	NM_001202429.2(ASB2):c.349G>A (p.Asp117Asn)	ASB2 (D117N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401304	NM_001202429.2(ASB2):c.341A>G (p.Lys114Arg)	ASB2 (K66R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260282	NM_001202429.2(ASB2):c.249G>A (p.Met83Ile)	ASB2 (M83I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589377	NM_001202429.2(ASB2):c.247A>G (p.Met83Val)	ASB2 (M35V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511246	NM_001202429.2(ASB2):c.233C>T (p.Pro78Leu)	ASB2 (P30L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130170	NM_001202429.2(ASB2):c.209C>T (p.Ser70Phe)	ASB2 (S70F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 61