Details for GHR:c.1449C>G, p.Ser483Arg

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
4271903742718935
VARIANT EFFECT None
ANNOTATION FLAG None
GENE GHR
REFERENCE ALLELE C
ALTERNATE ALLELE G
TRANSCRIPT NM_001242399
CDNA CHANGE c.1449C>G
PROTEIN CHANGE p.Ser483Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.176542Polymorphism
DBSNP ID NA
1 combination linked to GHR:c.1449C>G, p.Ser483Arg OLI1559
1 disease linked to GHR:c.1449C>G, p.Ser483Arg Syndrome with 46,XY disorder of sex development

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