5-140822061-C-A
Variant summary
Our verdict is Likely benign. The variant received -1 ACMG points: 2P and 3B. PM2BP4_ModerateBP7
The NM_018908.3(PCDHA5):c.286C>A(p.Arg96Arg) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000342 in 1,461,846 control chromosomes in the GnomAD database, with no homozygous occurrence. 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_018908.3 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_018908.3. 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 |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA5 | MANE Select | c.286C>A | p.Arg96Arg | synonymous | Exon 1 of 4 | NP_061731.1 | Q9Y5H7-1 | ||
| PCDHA1 | MANE Select | c.2394+33377C>A | intron | N/A | NP_061723.1 | Q9Y5I3-1 | |||
| PCDHA3 | MANE Select | c.2394+18470C>A | intron | N/A | NP_061729.1 | Q9Y5H8-1 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA5 | TSL:1 MANE Select | c.286C>A | p.Arg96Arg | synonymous | Exon 1 of 4 | ENSP00000436557.1 | Q9Y5H7-1 | ||
| PCDHA5 | TSL:1 | c.286C>A | p.Arg96Arg | synonymous | Exon 1 of 5 | ENSP00000433416.1 | Q9Y5H7-3 | ||
| PCDHA1 | TSL:1 MANE Select | c.2394+33377C>A | intron | N/A | ENSP00000420840.3 | Q9Y5I3-1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD2 exomes AF: 0.0000199 AC: 5AN: 251390 AF XY: 0.0000147 show subpopulations
GnomAD4 exome AF: 0.00000342 AC: 5AN: 1461846Hom.: 0 Cov.: 35 AF XY: 0.00000413 AC XY: 3AN XY: 727216 show subpopulations
Age Distribution
GnomAD4 genome Cov.: 33
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at