Details for BBS9:c.1789C>T, p.Gln597Ter

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
3340747433367862
VARIANT EFFECT None
ANNOTATION FLAG None
GENE BBS9
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_198428.3
CDNA CHANGE c.1789C>T
PROTEIN CHANGE p.Gln597Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone8.390444Disease causing
DBSNP ID NA
1 combination linked to BBS9:c.1789C>T, p.Gln597Ter OLI1452
1 disease linked to BBS9:c.1789C>T, p.Gln597Ter Bardet-Biedl syndrome

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