5-140807577-G-A
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_018907.4(PCDHA4):c.390G>A(p.Pro130Pro) 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. Synonymous variant affecting the same amino acid position (i.e. P130P) has been classified as Likely benign.
Frequency
Consequence
NM_018907.4 synonymous
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_018907.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA4 | MANE Select | c.390G>A | p.Pro130Pro | synonymous | Exon 1 of 4 | NP_061730.1 | Q9UN74-1 | ||
| PCDHA1 | MANE Select | c.2394+18893G>A | intron | N/A | NP_061723.1 | Q9Y5I3-1 | |||
| PCDHA3 | MANE Select | c.2394+3986G>A | intron | N/A | NP_061729.1 | Q9Y5H8-1 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| PCDHA4 | TSL:1 MANE Select | c.390G>A | p.Pro130Pro | synonymous | Exon 1 of 4 | ENSP00000435300.1 | Q9UN74-1 | ||
| PCDHA4 | TSL:1 | c.390G>A | p.Pro130Pro | synonymous | Exon 1 of 5 | ENSP00000423470.2 | D6RA20 | ||
| PCDHA1 | TSL:1 MANE Select | c.2394+18893G>A | intron | N/A | ENSP00000420840.3 | Q9Y5I3-1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 126
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at