ClinVar Genomic variation as it relates to human health
NM_018899.6(PCDHAC2):c.1904T>C (p.Val635Ala)
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
PCDHA1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 1149 | |
PCDHA10 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 466 | |
PCDHA11 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 378 | |
PCDHA12 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 307 | |
PCDHA13 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 209 | |
PCDHA2 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 1083 | |
PCDHA3 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 1012 | |
PCDHA4 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 934 | |
PCDHA5 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 880 | |
PCDHA6 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 814 |
There are 6 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 10, 2022 | RCV004125849.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024