NM_018917.4:c.292G>T
Variant summary
Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2BP4
The NM_018917.4(PCDHGA4):c.292G>T(p.Val98Phe) 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 1,461,716 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. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. V98L) has been classified as Uncertain significance.
Frequency
Consequence
NM_018917.4 missense
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Uncertain_significance. The variant received 1 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_018917.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| PCDHGA4 | NM_018917.4 | MANE Select | c.292G>T | p.Val98Phe | missense | Exon 1 of 4 | NP_061740.2 | Q9Y5G9-1 | |
| PCDHGA2 | NM_018915.4 | MANE Select | c.2424+14004G>T | intron | N/A | NP_061738.1 | Q9Y5H1-1 | ||
| PCDHGA3 | NM_018916.4 | MANE Select | c.2424+8942G>T | intron | N/A | NP_061739.2 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| PCDHGA4 | ENST00000571252.3 | TSL:1 MANE Select | c.292G>T | p.Val98Phe | missense | Exon 1 of 4 | ENSP00000458570.2 | Q9Y5G9-1 | |
| PCDHGA3 | ENST00000253812.8 | TSL:1 MANE Select | c.2424+8942G>T | intron | N/A | ENSP00000253812.7 | Q9Y5H0-1 | ||
| PCDHGA2 | ENST00000394576.3 | TSL:1 MANE Select | c.2424+14004G>T | intron | N/A | ENSP00000378077.2 | Q9Y5H1-1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD4 exome AF: 6.84e-7 AC: 1AN: 1461716Hom.: 0 Cov.: 32 AF XY: 0.00000138 AC XY: 1AN XY: 727140 show subpopulations
GnomAD4 genome Cov.: 33
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at