Details for FGFR1:c.1037_1038delCT, p.Ser346TyrfsTer61

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
3827945038421932
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FGFR1
REFERENCE ALLELE ACT
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.1037_1038delCT
PROTEIN CHANGE p.Ser346TyrfsTer61
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNoneNoneDisease causing
DBSNP ID NA
1 combination linked to FGFR1:c.1037_1038delCT, p.Ser346TyrfsTer61 OLI1376
1 disease linked to FGFR1:c.1037_1038delCT, p.Ser346TyrfsTer61 Hypogonadotropic hypogonadism with Fertile Eunuch phenotype

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