Details for KRT5:c.1261G>A, p.Gly421Arg

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
5291059952516815
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE KRT5
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_000424.3
CDNA CHANGE c.1261G>A
PROTEIN CHANGE p.Gly421Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.507156Disease causing
DBSNP ID NA
1 combination linked to KRT5:c.1261G>A, p.Gly421Arg OLI517
1 disease linked to KRT5:c.1261G>A, p.Gly421Arg Epidermolysis bullosa simplex

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