Details for GNRHR:c.636C>G, p.Asn212Lys

CHROMOSOME 4
GENOMIC COORDINATES
hg19hg38
6861039267744674
VARIANT EFFECT None
ANNOTATION FLAG None
GENE GNRHR
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.636C>G
PROTEIN CHANGE p.Asn212Lys
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.138068Polymorphism
DBSNP ID NA
1 combination linked to GNRHR:c.636C>G, p.Asn212Lys OLI1385
1 disease linked to GNRHR:c.636C>G, p.Asn212Lys Hypogonadotropic hypogonadism with partial puberty phenotype

Found any issues with the data on this page? Report this entry.