Details for FGFR1:p.Trp190Ter

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
3828549138427973
VARIANT EFFECT nonsense
ANNOTATION FLAG automatically_attributed
GENE FGFR1
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE p.Trp190Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone7.731416Disease causing
DBSNP ID rs1554567027
1 combination linked to FGFR1:p.Trp190Ter OLI356
1 disease linked to FGFR1:p.Trp190Ter Kallmann syndrome

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