Details for EDA:c.936C>G, p.Ile312Met

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
6925521970035369
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE EDA
REFERENCE ALLELE C
ALTERNATE ALLELE G
TRANSCRIPT NM_001399.4
CDNA CHANGE c.936C>G
PROTEIN CHANGE p.Ile312Met
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.244179Disease causing
DBSNP ID NA
1 combination linked to EDA:c.936C>G, p.Ile312Met OLI160
1 disease linked to EDA:c.936C>G, p.Ile312Met Hypodontia

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