Variant #0000467907 (NC_000001.10:g.147232740C>T, NC_000001.10(NM_005266.6):c.-33-1361G>A (GJA5))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.147232740C>T |
| DNA change (hg38) |
g.147760632= |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GJA5_000012 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs10465885 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.41-0.63 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2012-11-25 13:22:08 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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