Details for NPHP4:c.2126A>G, p.Asp709Gly

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
59646945904634
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NPHP4
REFERENCE ALLELE T
ALTERNATE ALLELE C
TRANSCRIPT NM_015102.3
CDNA CHANGE c.2126A>G
PROTEIN CHANGE p.Asp709Gly
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedDamaging2.825437Polymorphism
DBSNP ID NA
1 combination linked to NPHP4:c.2126A>G, p.Asp709Gly OLI1663
1 disease linked to NPHP4:c.2126A>G, p.Asp709Gly Bardet-Biedl syndrome

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