Variant #0000651418 (NC_000004.11:g.15504459T>G, NM_001080522.2:c.351T>G (CC2D2A))
Individual ID |
00293561 |
Chromosome |
4 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15504459T>G |
DNA change (hg38) |
g.15502836T>G |
Published as |
- |
ISCN |
- |
DB-ID |
CC2D2A_000045 See all 4 reported entries |
Variant remarks |
conflicting interpretations of pathogenicity; 8 heterozygous, no homozygous; Clinindb (India) |
Reference |
PubMed: Narang 2020, Journal: Narang 2020 |
ClinVar ID |
- |
dbSNP ID |
rs186264635 |
Origin |
Germline |
Segregation |
- |
Frequency |
8/2780 individuals |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00127 View details |
Owner |
Mohammed Faruq |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2020-03-11 19:46:11 +01:00 (CET) |
Date last edited |
2022-02-12 07:03:07 +01:00 (CET) |

Variant on transcripts
Screenings
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