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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 32

	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 3292448	NM_001321739.2(M1AP):c.1214T>C (p.Leu405Pro)	M1AP (L405P)	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 3292449	NM_001321739.2(M1AP):c.460G>A (p.Val154Met)	M1AP (V154M)	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 3292447	NM_001321739.2(M1AP):c.86T>C (p.Ile29Thr)	M1AP (I29T)	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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 32