Details for MSH4:c.1855A>G, p.Met619Val

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
7634700475881319
VARIANT EFFECT None
ANNOTATION FLAG None
GENE MSH4
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_002440.4
CDNA CHANGE c.1855A>G
PROTEIN CHANGE p.Met619Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00.00.00.00.00.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.388032Polymorphism
DBSNP ID NA
1 combination linked to MSH4:c.1855A>G, p.Met619Val OLI1726
1 disease linked to MSH4:c.1855A>G, p.Met619Val Primary ovarian failure

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