Details for MYH7:c.2645A>G, p.Gln882Arg

CHROMOSOME 14
GENOMIC COORDINATES
hg19hg38
2389401223424803
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE MYH7
REFERENCE ALLELE T
ALTERNATE ALLELE C
TRANSCRIPT NM_000257.3
CDNA CHANGE c.2645A>G
PROTEIN CHANGE p.Gln882Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.8748Disease causing
DBSNP ID NA
1 combination linked to MYH7:c.2645A>G, p.Gln882Arg OLI235
1 disease linked to MYH7:c.2645A>G, p.Gln882Arg Dilated cardiomyopathy

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