Details for BBS1:c.1338C>T, p.Thr446=

CHROMOSOME 11
GENOMIC COORDINATES
hg19hg38
6629427766526806
VARIANT EFFECT None
ANNOTATION FLAG None
GENE BBS1
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_024649.5
CDNA CHANGE c.1338C>T
PROTEIN CHANGE p.Thr446=
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00080.00.00.00.00.0041

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00039890.00.00.00.00.01.77e-050.0001630.003168

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone-0.251926Polymorphism
DBSNP ID rs368302072
1 combination linked to BBS1:c.1338C>T, p.Thr446= OLI1122
1 disease linked to BBS1:c.1338C>T, p.Thr446= Bardet-Biedl syndrome

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