chr8-38426242-G-T
Variant summary
Our verdict is Likely pathogenic. Variant got 9 ACMG points: 9P and 0B. PM1PM2PM5PP2PP3_Moderate
The NM_023110.3(FGFR1):c.625C>A(p.Arg209Ser) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R209C) has been classified as Likely pathogenic.
Frequency
Consequence
NM_023110.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_pathogenic. Variant got 9 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
FGFR1 | NM_023110.3 | c.625C>A | p.Arg209Ser | missense_variant | 6/18 | ENST00000447712.7 | NP_075598.2 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
FGFR1 | ENST00000447712.7 | c.625C>A | p.Arg209Ser | missense_variant | 6/18 | 1 | NM_023110.3 | ENSP00000400162.2 | ||
FGFR1 | ENST00000397091.9 | c.619C>A | p.Arg207Ser | missense_variant | 6/18 | 1 | ENSP00000380280.5 | |||
FGFR1 | ENST00000397108.8 | c.619C>A | p.Arg207Ser | missense_variant | 7/19 | 1 | ENSP00000380297.4 | |||
FGFR1 | ENST00000397113.6 | c.619C>A | p.Arg207Ser | missense_variant | 6/18 | 2 | ENSP00000380302.2 | |||
FGFR1 | ENST00000356207.9 | c.358C>A | p.Arg120Ser | missense_variant | 5/17 | 1 | ENSP00000348537.5 | |||
FGFR1 | ENST00000397103.5 | c.352C>A | p.Arg118Ser | missense_variant | 4/16 | 5 | ENSP00000380292.1 | |||
FGFR1 | ENST00000326324.10 | c.352C>A | p.Arg118Ser | missense_variant | 5/17 | 1 | ENSP00000327229.6 | |||
FGFR1 | ENST00000487647.5 | n.*316C>A | non_coding_transcript_exon_variant | 5/12 | 1 | ENSP00000435254.1 | ||||
FGFR1 | ENST00000487647.5 | n.*316C>A | 3_prime_UTR_variant | 5/12 | 1 | ENSP00000435254.1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 31
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.