Details for IGSF10:c.1786C>T, p.His596Tyr

CHROMOSOME 3
GENOMIC COORDINATES
hg19hg38
151165983151448195
VARIANT EFFECT None
ANNOTATION FLAG None
GENE IGSF10
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.1786C>T
PROTEIN CHANGE p.His596Tyr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.978e-060.00.00.00.00.08.797e-060.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign0.09508Polymorphism
DBSNP ID NA
1 combination linked to IGSF10:c.1786C>T, p.His596Tyr OLI1387
1 disease linked to IGSF10:c.1786C>T, p.His596Tyr Hypogonadotropic hypogonadism with partial puberty phenotype

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