"Ambry Genetics"[submitter] AND "INO80B"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2270815	NM_031288.4(INO80B):c.559G>T (p.Ala187Ser)	INO80B-WBP1, INO80B (A187S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2366318	NM_031288.4(INO80B):c.571C>T (p.Pro191Ser)	INO80B-WBP1, INO80B (P191S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2290164	NM_031288.4(INO80B):c.913C>G (p.Pro305Ala)	INO80B-WBP1, INO80B (P305A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2406425	NM_031288.4(INO80B):c.953G>T (p.Arg318Leu)	INO80B-WBP1, INO80B (R318L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance