Details for BBS10:c.1907C>T, p.Ala636Val

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
7673985876346078
VARIANT EFFECT None
ANNOTATION FLAG None
GENE BBS10
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_024685.4
CDNA CHANGE c.1907C>T
PROTEIN CHANGE p.Ala636Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.823092Disease causing
DBSNP ID rs113224628
1 combination linked to BBS10:c.1907C>T, p.Ala636Val OLI1127
1 disease linked to BBS10:c.1907C>T, p.Ala636Val Bardet-Biedl syndrome

Found any issues with the data on this page? Report this entry.