Details for BBS4:c.1508C>T, p.Pro503Leu

CHROMOSOME 15
GENOMIC COORDINATES
hg19hg38
7302987672737535
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE BBS4
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT ENST00000268057.9
CDNA CHANGE c.1508C>T
PROTEIN CHANGE p.Pro503Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign3.174797Disease causing
DBSNP ID rs756419611
1 combination linked to BBS4:c.1508C>T, p.Pro503Leu OLI124
1 disease linked to BBS4:c.1508C>T, p.Pro503Leu Bardet-Biedl syndrome

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