Variant #0000931433 (NC_000023.10:g.49840588A>G, NM_001127898.3:c.554A>G (CLCN5))
Chromosome |
X |
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.49840588A>G |
DNA change (hg38) |
- |
Published as |
CLCN5(NM_000084.2):c.344A>G (p.(Lys115Arg)), CLCN5(NM_000084.5):c.344A>G (p.K115R), CLCN5(NM_001127899.3):c.554A>G (p.K185R) |
ISCN |
- |
DB-ID |
CLCN5_000122 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) |
0.00035 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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