"Ambry Genetics"[submitter] AND "INO80C"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109755	NM_194281.4(INO80C):c.568A>G (p.Ile190Val)	INO80C (I135V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348262	NM_194281.4(INO80C):c.532G>A (p.Val178Ile)	INO80C (V123I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286049	NM_194281.4(INO80C):c.508A>T (p.Ile170Phe)	INO80C (I115F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290265	NM_194281.4(INO80C):c.478C>T (p.Arg160Trp)	INO80C (R196W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603103	NM_194281.4(INO80C):c.398C>T (p.Pro133Leu)	INO80C, LOC126862726 (P133L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401821	NM_194281.4(INO80C):c.217C>T (p.Pro73Ser)	INO80C (P109S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330951	NM_194281.4(INO80C):c.193G>T (p.Val65Leu)	INO80C (V65L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286050	NM_194281.4(INO80C):c.157G>A (p.Gly53Ser)	INO80C (G53S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347691	NM_194281.4(INO80C):c.146G>A (p.Ser49Asn)	INO80C (S49N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109753	NM_194281.4(INO80C):c.142T>C (p.Ser48Pro)	INO80C (S48P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222312	NM_194281.4(INO80C):c.142T>G (p.Ser48Ala)	INO80C (S48A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286048	NM_194281.4(INO80C):c.136T>G (p.Ser46Ala)	INO80C (S46A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284475	NM_194281.4(INO80C):c.110A>C (p.Tyr37Ser)	INO80C (Y37S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109756	NM_194281.4(INO80C):c.76A>T (p.Ser26Cys)	INO80C (S26C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607294	NM_194281.4(INO80C):c.68G>A (p.Arg23Lys)	INO80C (R23K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512755	NM_194281.4(INO80C):c.59G>A (p.Ser20Asn)	INO80C (S20N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264257	NM_194281.4(INO80C):c.41C>T (p.Pro14Leu)	INO80C (P14L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109754	NM_194281.4(INO80C):c.20T>C (p.Ile7Thr)	INO80C (I7T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance