Details for PROKR2:c.253C>T, p.Arg85Cys

CHROMOSOME 20
GENOMIC COORDINATES
hg19hg38
52947635314117
VARIANT EFFECT None
ANNOTATION FLAG None
GENE PROKR2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_144773.4
CDNA CHANGE c.253C>T
PROTEIN CHANGE p.Arg85Cys
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00060.00080.00140.00.0010.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00059250.0012920.0014170.0020830.00021750.00.00036920.0019540.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.012438Disease causing
DBSNP ID NA
7 combinations linked to PROKR2:c.253C>T, p.Arg85Cys OLI1297; OLI1525; OLI1544; OLI1547; OLI1548; OLI1558; OLI1567
3 diseases linked to PROKR2:c.253C>T, p.Arg85Cys 46,XY disorder of sex development; Kallmann syndrome; Syndrome with 46,XY disorder of sex development

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