Details for BBS2:c.117+1G>C,

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
5655365756519745
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE BBS2
REFERENCE ALLELE C
ALTERNATE ALLELE G
TRANSCRIPT NM_031885.5
CDNA CHANGE c.117+1G>C
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone6.374925Disease causing
DBSNP ID NA
1 combination linked to BBS2:c.117+1G>C, OLI064
1 disease linked to BBS2:c.117+1G>C, Bardet-Biedl syndrome

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