rs1372591495
Variant summary
Our verdict is Likely benign. The variant received -1 ACMG points: 2P and 3B. PM2BP4_ModerateBP7
The NM_018916.4(PCDHGA3):c.274C>A(p.Arg92Arg) 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_018916.4 synonymous
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -1 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_018916.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| PCDHGA3 | NM_018916.4 | MANE Select | c.274C>A | p.Arg92Arg | synonymous | Exon 1 of 4 | NP_061739.2 | ||
| PCDHGA2 | NM_018915.4 | MANE Select | c.2424+2912C>A | intron | N/A | NP_061738.1 | Q9Y5H1-1 | ||
| PCDHGA1 | NM_018912.3 | MANE Select | c.2421+11202C>A | intron | N/A | NP_061735.1 | Q9Y5H4-1 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| PCDHGA3 | ENST00000253812.8 | TSL:1 MANE Select | c.274C>A | p.Arg92Arg | synonymous | Exon 1 of 4 | ENSP00000253812.7 | Q9Y5H0-1 | |
| PCDHGA2 | ENST00000394576.3 | TSL:1 MANE Select | c.2424+2912C>A | intron | N/A | ENSP00000378077.2 | Q9Y5H1-1 | ||
| PCDHGA1 | ENST00000517417.3 | TSL:1 MANE Select | c.2421+11202C>A | intron | N/A | ENSP00000431083.1 | Q9Y5H4-1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD2 exomes AF: 0.00000400 AC: 1AN: 249712 AF XY: 0.00000738 show subpopulations
GnomAD4 exome Cov.: 32
GnomAD4 genome Cov.: 33
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at