"Ambry Genetics"[submitter] AND "M1AP"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2367463	NM_001321739.2(M1AP):c.1415C>T (p.Pro472Leu)	M1AP (P472L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2237001	NM_001321739.2(M1AP):c.1414C>T (p.Pro472Ser)	M1AP (P472S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356854	NM_001321739.2(M1AP):c.1409G>A (p.Arg470Gln)	M1AP (R470Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612045	NM_001321739.2(M1AP):c.1306G>C (p.Glu436Gln)	M1AP (E436Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372423	NM_001321739.2(M1AP):c.1276G>A (p.Val426Met)	M1AP (V426M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383025	NM_001321739.2(M1AP):c.1205C>T (p.Thr402Met)	M1AP (T402M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474724	NM_001321739.2(M1AP):c.971A>G (p.Tyr324Cys)	M1AP (Y324C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121816	NM_001321739.2(M1AP):c.842T>G (p.Leu281Trp)	M1AP (L281W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383279	NM_001321739.2(M1AP):c.839C>T (p.Ser280Phe)	M1AP (S280F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121815	NM_001321739.2(M1AP):c.773G>A (p.Cys258Tyr)	M1AP (C258Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121814	NM_001321739.2(M1AP):c.771G>A (p.Met257Ile)	M1AP (M257I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377354	NM_001321739.2(M1AP):c.649G>A (p.Val217Ile)	M1AP (V217I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121813	NM_001321739.2(M1AP):c.602C>G (p.Ser201Cys)	M1AP (S201C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608670	NM_001321739.2(M1AP):c.557T>A (p.Val186Glu)	M1AP (V186E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121812	NM_001321739.2(M1AP):c.502G>A (p.Ala168Thr)	M1AP (A168T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312716	NM_001321739.2(M1AP):c.437T>C (p.Leu146Pro)	M1AP (L146P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121811	NM_001321739.2(M1AP):c.394A>G (p.Thr132Ala)	M1AP (T132A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245280	NM_001321739.2(M1AP):c.337C>T (p.Arg113Trp)	M1AP (R113W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324813	NM_001321739.2(M1AP):c.325G>A (p.Gly109Ser)	M1AP (G109S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258752	NM_001321739.2(M1AP):c.293T>C (p.Met98Thr)	M1AP (M98T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535237	NM_001321739.2(M1AP):c.275G>C (p.Cys92Ser)	M1AP (C92S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121810	NM_001321739.2(M1AP):c.274T>G (p.Cys92Gly)	M1AP (C92G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121809	NM_001321739.2(M1AP):c.254A>G (p.Asn85Ser)	M1AP (N85S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374273	NM_001321739.2(M1AP):c.197T>C (p.Leu66Ser)	M1AP (L66S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382440	NM_001321739.2(M1AP):c.179G>A (p.Arg60His)	M1AP (R60H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121807	NM_001321739.2(M1AP):c.125G>A (p.Cys42Tyr)	M1AP (C42Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383306	NM_001321739.2(M1AP):c.44C>T (p.Thr15Ile)	M1AP (T15I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524382	NM_001321739.2(M1AP):c.37A>G (p.Thr13Ala)	M1AP (T13A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257478	NM_001321739.2(M1AP):c.5A>T (p.His2Leu)	M1AP (H2L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29