Details for COBL:c.1538C>T, p.Ser513Phe

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
5111111951043422
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE COBL
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001346443.1
CDNA CHANGE c.1538C>T
PROTEIN CHANGE p.Ser513Phe
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.890494Polymorphism
DBSNP ID NA
1 combination linked to COBL:c.1538C>T, p.Ser513Phe OLI750
1 disease linked to COBL:c.1538C>T, p.Ser513Phe Isolated anencephaly

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