Details for BBS10:c.1867C>T, p.Gln623Ter

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
7673989876346118
VARIANT EFFECT nonsense
ANNOTATION FLAG automatically_attributed
GENE BBS10
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_024685.3
CDNA CHANGE c.1867C>T
PROTEIN CHANGE p.Gln623Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone6.348651Disease causing
DBSNP ID NA
1 combination linked to BBS10:c.1867C>T, p.Gln623Ter OLI176
1 disease linked to BBS10:c.1867C>T, p.Gln623Ter Bardet-Biedl syndrome

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