NM_018917.4:c.364G>C
Variant summary
Our verdict is Uncertain significance. The variant received 4 ACMG points: 4P and 0B. PM2PP3_Moderate
The NM_018917.4(PCDHGA4):c.364G>C(p.Asp122His) variant causes a missense change involving the alteration of a conserved nucleotide. The variant allele was found at a frequency of 0.00000205 in 1,461,722 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar 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 4 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.364G>C | p.Asp122His | missense | Exon 1 of 4 | NP_061740.2 | Q9Y5G9-1 | |
| PCDHGA2 | NM_018915.4 | MANE Select | c.2424+14076G>C | intron | N/A | NP_061738.1 | Q9Y5H1-1 | ||
| PCDHGA3 | NM_018916.4 | MANE Select | c.2424+9014G>C | 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.364G>C | p.Asp122His | missense | Exon 1 of 4 | ENSP00000458570.2 | Q9Y5G9-1 | |
| PCDHGA3 | ENST00000253812.8 | TSL:1 MANE Select | c.2424+9014G>C | intron | N/A | ENSP00000253812.7 | Q9Y5H0-1 | ||
| PCDHGA2 | ENST00000394576.3 | TSL:1 MANE Select | c.2424+14076G>C | intron | N/A | ENSP00000378077.2 | Q9Y5H1-1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD4 exome AF: 0.00000205 AC: 3AN: 1461722Hom.: 0 Cov.: 32 AF XY: 0.00000275 AC XY: 2AN XY: 727144 show subpopulations
Age Distribution
GnomAD4 genome Cov.: 33
ClinVar
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at