Details for NBN:c.596C>G, p.Pro199Arg

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
9098350789971279
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NBN
REFERENCE ALLELE G
ALTERNATE ALLELE C
TRANSCRIPT N.A.
CDNA CHANGE c.596C>G
PROTEIN CHANGE p.Pro199Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.876092Polymorphism
DBSNP ID NA
1 combination linked to NBN:c.596C>G, p.Pro199Arg OLI1058
1 disease linked to NBN:c.596C>G, p.Pro199Arg Primary ovarian failure

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