Variant #0000927499 (NC_000016.9:g.1506192G>A, NM_001287.5:c.838C>T (CLCN7))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1506192G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
CLCN7_000053 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1395527274 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2023-04-28 09:39:01 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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