ClinVar for Gene (Select 100532735) - ClinVar

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Links from Gene

Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3189686	NM_012477.4(WBP1):c.761C>T (p.Pro254Leu)	INO80B-WBP1, WBP1 (P254L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3189685	NM_012477.4(WBP1):c.646C>T (p.Leu216Phe)	INO80B-WBP1, WBP1 (L216F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3189684	NM_012477.4(WBP1):c.610C>T (p.Arg204Cys)	INO80B-WBP1, WBP1 (R204C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3189683	NM_012477.4(WBP1):c.31G>A (p.Glu11Lys)	INO80B-WBP1, WBP1 (E11K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189682	NM_012477.4(WBP1):c.265C>T (p.Arg89Trp)	INO80B-WBP1, WBP1 (R89W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3189681	NM_012477.4(WBP1):c.117G>C (p.Glu39Asp)	INO80B-WBP1, WBP1 (E39D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109752	NM_031288.4(INO80B):c.83C>T (p.Ala28Val)	INO80B, INO80B-WBP1 (A28V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109751	NM_031288.4(INO80B):c.577C>T (p.Pro193Ser)	INO80B, INO80B-WBP1 (P193S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109750	NM_031288.4(INO80B):c.22G>A (p.Gly8Arg)	INO80B, INO80B-WBP1 +1 more (G8R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109749	NM_031288.4(INO80B):c.199C>T (p.Pro67Ser)	INO80B, INO80B-WBP1 (P67S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109748	NM_031288.4(INO80B):c.1061T>G (p.Leu354Trp)	INO80B, INO80B-WBP1 (L354W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2606391	NM_012477.4(WBP1):c.103C>T (p.Pro35Ser)	INO80B-WBP1, WBP1 (P35S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2555962	NM_031288.4(INO80B):c.902C>G (p.Ser301Cys)	INO80B, INO80B-WBP1 (S301C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2555836	NM_031288.4(INO80B):c.86G>A (p.Gly29Asp)	INO80B, INO80B-WBP1 (G29D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2551154	NM_012477.4(WBP1):c.328A>G (p.Thr110Ala)	INO80B-WBP1, WBP1 (T110A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2547595	NM_031288.4(INO80B):c.770C>T (p.Ala257Val)	INO80B, INO80B-WBP1 +1 more (A257V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2541315	NM_031288.4(INO80B):c.736G>A (p.Ala246Thr)	INO80B, INO80B-WBP1 +1 more (A246T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2538568	NM_031288.4(INO80B):c.563G>A (p.Arg188Gln)	INO80B, INO80B-WBP1 (R188Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2520996	NM_031288.4(INO80B):c.916C>T (p.Pro306Ser)	INO80B, INO80B-WBP1 (P306S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2484759	NM_031288.4(INO80B):c.517G>A (p.Glu173Lys)	INO80B, INO80B-WBP1 (E173K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2483346	NM_031288.4(INO80B):c.919C>T (p.Pro307Ser)	INO80B, INO80B-WBP1 (P307S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2470447	NM_031288.4(INO80B):c.172G>A (p.Gly58Arg)	INO80B, INO80B-WBP1 (G58R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2467646	NM_031288.4(INO80B):c.823T>C (p.Tyr275His)	INO80B, INO80B-WBP1 +1 more (Y275H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2406425	NM_031288.4(INO80B):c.953G>T (p.Arg318Leu)	INO80B, INO80B-WBP1 (R318L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2379653	NM_012477.4(WBP1):c.226C>T (p.Arg76Cys)	INO80B-WBP1, WBP1 (R76C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2366318	NM_031288.4(INO80B):c.571C>T (p.Pro191Ser)	INO80B, INO80B-WBP1 (P191S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2366143	NM_012477.4(WBP1):c.682G>T (p.Val228Phe)	INO80B-WBP1, WBP1 (V228F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2362645	NM_012477.4(WBP1):c.619C>T (p.Arg207Cys)	INO80B-WBP1, WBP1 (R207C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2353112	NM_012477.4(WBP1):c.119G>A (p.Ser40Asn)	INO80B-WBP1, WBP1 (S40N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2334393	NM_012477.4(WBP1):c.418C>T (p.Pro140Ser)	INO80B-WBP1, WBP1 (P140S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2304382	NM_031288.4(INO80B):c.907T>A (p.Ser303Thr)	INO80B, INO80B-WBP1 (S303T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2292625	NM_012477.4(WBP1):c.542G>C (p.Ser181Thr)	INO80B-WBP1, WBP1 (S181T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2291290	NM_031288.4(INO80B):c.512T>C (p.Ile171Thr)	INO80B, INO80B-WBP1 (I171T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2290164	NM_031288.4(INO80B):c.913C>G (p.Pro305Ala)	INO80B, INO80B-WBP1 (P305A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2286533	NM_031288.4(INO80B):c.802G>A (p.Ala268Thr)	INO80B, INO80B-WBP1 +1 more (A268T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2281934	NM_012477.4(WBP1):c.617G>A (p.Arg206His)	INO80B-WBP1, WBP1 (R206H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2270815	NM_031288.4(INO80B):c.559G>T (p.Ala187Ser)	INO80B, INO80B-WBP1 (A187S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2265799	NM_031288.4(INO80B):c.814A>T (p.Met272Leu)	INO80B, INO80B-WBP1 +1 more (M272L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2256900	NM_012477.4(WBP1):c.805C>T (p.Pro269Ser)	INO80B-WBP1, WBP1 (P269S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250985	NM_012477.4(WBP1):c.462A>T (p.Glu154Asp)	INO80B-WBP1, WBP1 (E154D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2237716	NM_012477.4(WBP1):c.233G>A (p.Arg78Gln)	INO80B-WBP1, WBP1 (R78Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 155389	GRCh38/hg38 2p13.1-12(chr2:74375779-75517520)x1	AUP1, C2orf81 +86 more	Copy number loss	See cases	GLikely pathogenic
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	LOC126806252, LOC126806253 +2457 more	Copy number gain	See cases	GBenign
Select item 147468	GRCh38/hg38 2p13.1-12(chr2:74432069-75181627)x3	AUP1, CCDC142 +66 more	Copy number gain	See cases	GUncertain significance
Select item 146814	GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3	AAK1, ACTG2 +768 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 45