Variant #0000016463 (NC_000004.11:g.15599090T>A, NC_000004.11(NM_001080522.2):c.4496+2T>A (CC2D2A))
Chromosome |
4 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15599090T>A |
DNA change (hg38) |
g.15597467T>A |
Published as |
- |
ISCN |
- |
DB-ID |
CC2D2A_000021 See all 4 reported entries |
Variant remarks |
1 French MKS6 family (com-het); potential missplicing |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-11-15 14:05:58 +01:00 (CET) |
Date last edited |
2020-06-16 12:41:11 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|