Details for KRT14:c.380C>T, p.Ala127Val

CHROMOSOME 17
GENOMIC COORDINATES
hg19hg38
3974270741586455
VARIANT EFFECT missense
ANNOTATION FLAG manually_corrected
GENE KRT14
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000526.4
CDNA CHANGE c.380C>T
PROTEIN CHANGE p.Ala127Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.572477Disease causing
DBSNP ID NA
1 combination linked to KRT14:c.380C>T, p.Ala127Val OLI517
1 disease linked to KRT14:c.380C>T, p.Ala127Val Epidermolysis bullosa simplex

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