Details for NPHP3:c.362C>G, p.Thr121Arg

CHROMOSOME 3
GENOMIC COORDINATES
hg19hg38
132440838132721994
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE NPHP3
REFERENCE ALLELE G
ALTERNATE ALLELE C
TRANSCRIPT NM_153240.4
CDNA CHANGE c.362C>G
PROTEIN CHANGE p.Thr121Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign1.744625Disease causing
DBSNP ID NA
1 combination linked to NPHP3:c.362C>G, p.Thr121Arg OLI212
1 disease linked to NPHP3:c.362C>G, p.Thr121Arg Nephronophthisis

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