rs782374670
Variant summary
Our verdict is Likely benign. The variant received -3 ACMG points: 2P and 5B. PM2BP4_StrongBP7
The NM_018909.4(PCDHA6):c.243T>C(p.Asn81Asn) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000205 in 1,461,868 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_018909.4 synonymous
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -3 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_018909.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA6 | NM_018909.4 | MANE Select | c.243T>C | p.Asn81Asn | synonymous | Exon 1 of 4 | NP_061732.1 | Q9UN73-1 | |
| PCDHA1 | NM_018900.4 | MANE Select | c.2394+39650T>C | intron | N/A | NP_061723.1 | Q9Y5I3-1 | ||
| PCDHA3 | NM_018906.3 | MANE Select | c.2394+24743T>C | intron | N/A | NP_061729.1 | Q9Y5H8-1 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA6 | ENST00000529310.6 | TSL:1 MANE Select | c.243T>C | p.Asn81Asn | synonymous | Exon 1 of 4 | ENSP00000433378.1 | Q9UN73-1 | |
| PCDHA6 | ENST00000527624.1 | TSL:1 | c.243T>C | p.Asn81Asn | synonymous | Exon 1 of 4 | ENSP00000434113.1 | Q9UN73-2 | |
| PCDHA1 | ENST00000504120.4 | TSL:1 MANE Select | c.2394+39650T>C | intron | N/A | ENSP00000420840.3 | Q9Y5I3-1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD2 exomes AF: 0.00000398 AC: 1AN: 251378 AF XY: 0.00000736 show subpopulations
GnomAD4 exome AF: 0.00000205 AC: 3AN: 1461868Hom.: 0 Cov.: 32 AF XY: 0.00000275 AC XY: 2AN XY: 727234 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