Variant #0000915734 (NC_000023.10:g.49845243T>C, NC_000023.10(NM_001127898.3):c.604-8T>C (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.49845243T>C |
DNA change (hg38) |
- |
Published as |
CLCN5(NM_000084.5):c.394-8T>C |
ISCN |
- |
DB-ID |
CLCN5_000174 |
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) |
2.0E-5 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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