Details for SPRY4:c.722C>T, p.Ser241Phe

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
141694021142314456
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SPRY4
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_030964.5
CDNA CHANGE c.722C>T
PROTEIN CHANGE p.Ser241Phe
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.206716Polymorphism
DBSNP ID NA
1 combination linked to SPRY4:c.722C>T, p.Ser241Phe OLI1277
1 disease linked to SPRY4:c.722C>T, p.Ser241Phe Normosmic congenital hypogonadotropic hypogonadism

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