Details for MSH4:c.1286A>T, p.Glu429Val

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
7633325475867569
VARIANT EFFECT None
ANNOTATION FLAG None
GENE MSH4
REFERENCE ALLELE A
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.1286A>T
PROTEIN CHANGE p.Glu429Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging4.865126Polymorphism
DBSNP ID NA
1 combination linked to MSH4:c.1286A>T, p.Glu429Val OLI1069
1 disease linked to MSH4:c.1286A>T, p.Glu429Val Primary ovarian failure

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