5-140822136-G-A
Variant summary
Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_018908.3(PCDHA5):c.361G>A(p.Ala121Thr) variant causes a missense change. The variant allele was found at a frequency of 0.000031 in 1,614,138 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_018908.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -2 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
PCDHA5 | NM_018908.3 | c.361G>A | p.Ala121Thr | missense_variant | Exon 1 of 4 | ENST00000529859.2 | NP_061731.1 | |
PCDHA1 | NM_018900.4 | c.2394+33452G>A | intron_variant | Intron 1 of 3 | ENST00000504120.4 | NP_061723.1 | ||
PCDHA3 | NM_018906.3 | c.2394+18545G>A | intron_variant | Intron 1 of 3 | ENST00000522353.3 | NP_061729.1 | ||
PCDHA2 | NM_018905.3 | c.2388+24784G>A | intron_variant | Intron 1 of 3 | ENST00000526136.2 | NP_061728.1 | ||
PCDHA4 | NM_018907.4 | c.2385+12564G>A | intron_variant | Intron 1 of 3 | ENST00000530339.2 | NP_061730.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
PCDHA5 | ENST00000529859.2 | c.361G>A | p.Ala121Thr | missense_variant | Exon 1 of 4 | 1 | NM_018908.3 | ENSP00000436557.1 | ||
PCDHA1 | ENST00000504120.4 | c.2394+33452G>A | intron_variant | Intron 1 of 3 | 1 | NM_018900.4 | ENSP00000420840.3 | |||
PCDHA3 | ENST00000522353.3 | c.2394+18545G>A | intron_variant | Intron 1 of 3 | 1 | NM_018906.3 | ENSP00000429808.2 | |||
PCDHA2 | ENST00000526136.2 | c.2388+24784G>A | intron_variant | Intron 1 of 3 | 1 | NM_018905.3 | ENSP00000431748.1 | |||
PCDHA4 | ENST00000530339.2 | c.2385+12564G>A | intron_variant | Intron 1 of 3 | 1 | NM_018907.4 | ENSP00000435300.1 |
Frequencies
GnomAD3 genomes AF: 0.000243 AC: 37AN: 152248Hom.: 0 Cov.: 33
GnomAD3 exomes AF: 0.0000477 AC: 12AN: 251482Hom.: 0 AF XY: 0.00000736 AC XY: 1AN XY: 135920
GnomAD4 exome AF: 0.00000889 AC: 13AN: 1461890Hom.: 0 Cov.: 35 AF XY: 0.00000550 AC XY: 4AN XY: 727244
GnomAD4 genome AF: 0.000243 AC: 37AN: 152248Hom.: 0 Cov.: 33 AF XY: 0.000215 AC XY: 16AN XY: 74384
ClinVar
Submissions by phenotype
not specified Uncertain:1
The c.361G>A (p.A121T) alteration is located in exon 1 (coding exon 1) of the PCDHA5 gene. This alteration results from a G to A substitution at nucleotide position 361, causing the alanine (A) at amino acid position 121 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at