11-5323876-G-T
Variant summary
Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_033180.5(OR51B2):c.422C>A(p.Ala141Glu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000684 in 1,461,644 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 14/19 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. A141V) has been classified as Uncertain significance.
Frequency
Consequence
NM_033180.5 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_033180.5. You can select a different transcript below to see updated ACMG assignments.
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| OR51B2 | TSL:6 MANE Select | c.422C>A | p.Ala141Glu | missense | Exon 1 of 1 | ENSP00000485407.1 | Q9Y5P1 | ||
| HBE1 | TSL:1 | c.-266-53720C>A | intron | N/A | ENSP00000292896.2 | P02100 | |||
| HBE1 | TSL:1 | c.-309-41925C>A | intron | N/A | ENSP00000369586.1 | P02100 |
Frequencies
GnomAD3 genomes Cov.: 31
GnomAD2 exomes AF: 0.00000399 AC: 1AN: 250518 AF XY: 0.00000739 show subpopulations
GnomAD4 exome AF: 6.84e-7 AC: 1AN: 1461644Hom.: 0 Cov.: 54 AF XY: 0.00000138 AC XY: 1AN XY: 727108 show subpopulations
GnomAD4 genome Cov.: 31
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at