Details for BBS7:c.601+2T>C, p.Gly201_Asp202ins15or16

CHROMOSOME 4
GENOMIC COORDINATES
hg19hg38
122776642121855487
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE BBS7
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_176824.3
CDNA CHANGE c.601+2T>C
PROTEIN CHANGE p.Gly201_Asp202ins15or16
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.407747Disease causing
DBSNP ID NA
2 combinations linked to BBS7:c.601+2T>C, p.Gly201_Asp202ins15or16 OLI097; OLI1124
1 disease linked to BBS7:c.601+2T>C, p.Gly201_Asp202ins15or16 Bardet-Biedl syndrome

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