Details for PDE6B:c.1055G>T, p.Gly352Val

CHROMOSOME 4
GENOMIC COORDINATES
hg19hg38
649791656002
VARIANT EFFECT None
ANNOTATION FLAG None
GENE PDE6B
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_000283.4
CDNA CHANGE c.1055G>T
PROTEIN CHANGE p.Gly352Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.993e-060.00.00.00.04.674e-050.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.080759Disease causing
DBSNP ID NA
1 combination linked to PDE6B:c.1055G>T, p.Gly352Val OLI1453
1 disease linked to PDE6B:c.1055G>T, p.Gly352Val Bardet-Biedl syndrome

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