NM_001004452.1:c.28T>C
Variant summary
Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_001004452.1(OR1J4):c.28T>C(p.Ser10Pro) 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. 15/22 in silico tools predict a benign 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. S10A) has been classified as Uncertain significance.
Frequency
Consequence
NM_001004452.1 missense
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Uncertain_significance. The variant received 0 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_001004452.1. 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 |
|---|---|---|---|---|---|---|---|---|---|
| OR1J4 | NM_001004452.1 | MANE Select | c.28T>C | p.Ser10Pro | missense | Exon 1 of 1 | NP_001004452.1 | A0A126GW06 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR1J4 | ENST00000340750.1 | TSL:6 MANE Select | c.28T>C | p.Ser10Pro | missense | Exon 1 of 1 | ENSP00000343521.1 | Q8NGS1 | |
| ENSG00000234156 | ENST00000431442.3 | TSL:3 | n.1362+16298T>C | intron | N/A | ||||
| ENSG00000234156 | ENST00000723589.1 | n.1044+49983T>C | intron | N/A |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 32
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at