1-158610969-G-C
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_003126.4(SPTA1):c.*295C>G variant causes a 3 prime UTR 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_003126.4 3_prime_UTR
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_003126.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| SPTA1 | NM_003126.4 | MANE Select | c.*295C>G | 3_prime_UTR | Exon 52 of 52 | NP_003117.2 | P02549-1 | ||
| OR10Z1 | NM_001004478.2 | MANE Select | c.*3589G>C | 3_prime_UTR | Exon 2 of 2 | NP_001004478.1 | A0A126GV63 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| SPTA1 | ENST00000643759.2 | MANE Select | c.*295C>G | 3_prime_UTR | Exon 52 of 52 | ENSP00000495214.1 | P02549-1 | ||
| OR10Z1 | ENST00000641002.1 | MANE Select | c.*3589G>C | 3_prime_UTR | Exon 2 of 2 | ENSP00000493003.1 | Q8NGY1 | ||
| SPTA1 | ENST00000485680.1 | TSL:3 | n.*239C>G | downstream_gene | N/A |
Frequencies
GnomAD3 genomes Cov.: 31
GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0AN: 158838Hom.: 0 Cov.: 2 AF XY: 0.00 AC XY: 0AN XY: 84262
GnomAD4 genome Cov.: 31
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at