Variant #0001024751 (NC_000003.11:g.184071135_184071137dup, NM_004366.5:c.1932_1934dup (CLCN2))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.184071135_184071137dup |
DNA change (hg38) |
- |
Published as |
CLCN2(NM_001171087.2):c.1881_1883dup (p.(Arg629dup)), CLCN2(NM_004366.6):c.1932_1934dupCCG (p.R646dup) |
ISCN |
- |
DB-ID |
CLCN2_000010 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2025-02-07 18:57:27 +01:00 (CET) |
Date last edited |
N/A |

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