19-45470873-C-T
Variant summary
Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2BP4
The NM_006732.3(FOSB):c.371C>T(p.Ser124Phe) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_006732.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 1 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
FOSB | NM_006732.3 | c.371C>T | p.Ser124Phe | missense_variant | Exon 2 of 4 | ENST00000353609.8 | NP_006723.2 | |
FOSB | NM_001114171.2 | c.371C>T | p.Ser124Phe | missense_variant | Exon 2 of 3 | NP_001107643.1 | ||
FOSB | NM_001411069.1 | c.371C>T | p.Ser124Phe | missense_variant | Exon 2 of 5 | NP_001397998.1 | ||
FOSB | XM_047438550.1 | c.371C>T | p.Ser124Phe | missense_variant | Exon 2 of 4 | XP_047294506.1 |
Ensembl
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 31
GnomAD4 genome Cov.: 32
ClinVar
Submissions by phenotype
not specified Uncertain:1
The c.371C>T (p.S124F) alteration is located in exon 2 (coding exon 2) of the FOSB gene. This alteration results from a C to T substitution at nucleotide position 371, causing the serine (S) at amino acid position 124 to be replaced by a phenylalanine (F). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.