4-83462497-C-G
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_139076.3(ABRAXAS1):c.1202G>C(p.Gly401Ala) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. G401V) has been classified as Uncertain significance.
Frequency
Consequence
NM_139076.3 missense
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_139076.3. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| ABRAXAS1 | NM_139076.3 | MANE Select | c.1202G>C | p.Gly401Ala | missense | Exon 9 of 9 | NP_620775.2 | Q6UWZ7-1 | |
| ABRAXAS1 | NM_001345962.2 | c.875G>C | p.Gly292Ala | missense | Exon 8 of 8 | NP_001332891.1 | Q6UWZ7-2 | ||
| MRPS18C | NM_016067.4 | MANE Select | c.*1300C>G | downstream_gene | N/A | NP_057151.1 | Q9Y3D5 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| ABRAXAS1 | ENST00000321945.12 | TSL:1 MANE Select | c.1202G>C | p.Gly401Ala | missense | Exon 9 of 9 | ENSP00000369857.3 | Q6UWZ7-1 | |
| ABRAXAS1 | ENST00000856950.1 | c.1190G>C | p.Gly397Ala | missense | Exon 9 of 9 | ENSP00000527009.1 | |||
| ABRAXAS1 | ENST00000856949.1 | c.1082G>C | p.Gly361Ala | missense | Exon 8 of 8 | ENSP00000527008.1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD4 exome Cov.: 30
GnomAD4 genome Cov.: 33
ClinVar
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at