Variant #0000071791 (NC_000013.10:g.20797144T>C, NM_006783.4:c.476A>G (GJB6))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.20797144T>C |
| DNA change (hg38) |
g.20223005T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GJB6_000018 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs35277762 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00052 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-06-19 09:43:09 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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