Details for FGFR1:c.1960G>T, p.Asp654Tyr

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
3827240738414889
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FGFR1
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_001174067
CDNA CHANGE c.1960G>T
PROTEIN CHANGE p.Asp654Tyr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.627957Disease causing
DBSNP ID NA
1 combination linked to FGFR1:c.1960G>T, p.Asp654Tyr OLI1559
1 disease linked to FGFR1:c.1960G>T, p.Asp654Tyr Syndrome with 46,XY disorder of sex development

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