6-29440777-A-G
Variant summary
Our verdict is Likely benign. The variant received -3 ACMG points: 2P and 5B. PM2BP4_StrongBP7
The NM_013941.4(OR10C1):c.762A>G(p.Ala254Ala) variant causes a synonymous 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_013941.4 synonymous
Scores
Clinical Significance
Conservation
Publications
Genome browser will be placed here
ACMG classification
Our verdict: Likely_benign. The variant received -3 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_013941.4. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR10C1 | NM_013941.4 | MANE Select | c.762A>G | p.Ala254Ala | synonymous | Exon 1 of 1 | NP_039229.3 | ||
| OR11A1 | NM_001394828.1 | MANE Select | c.-388-8790T>C | intron | N/A | NP_001381757.1 |
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR10C1 | ENST00000444197.3 | TSL:6 MANE Select | c.762A>G | p.Ala254Ala | synonymous | Exon 1 of 1 | ENSP00000419119.1 | ||
| OR11A1 | ENST00000377149.5 | TSL:6 MANE Select | c.-388-8790T>C | intron | N/A | ENSP00000366354.1 | |||
| OR10C1 | ENST00000622521.1 | TSL:6 | c.768A>G | p.Ala256Ala | synonymous | Exon 1 of 1 | ENSP00000481429.1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 34
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at