Variant #0001045891 (NC_000003.11:g.184069796_184069797dup, NC_000003.11(NM_004366.5):c.2415+5_2415+6dup (CLCN2))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.184069796_184069797dup |
| DNA change (hg38) |
- |
| Published as |
CLCN2(NM_001171087.2):c.2364+5_2364+6dup (p.?), CLCN2(NM_004366.6):c.2415+5_2415+6dupGG |
| ISCN |
- |
| DB-ID |
FAM131A_000002 See all 2 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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