Variant #0000990249 (NC_000001.10:g.147380823T>G, NM_005267.4:c.741T>G (GJA8))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.147380823T>G |
| DNA change (hg38) |
- |
| Published as |
GJA8(NM_005267.4):c.741T>G (p.I247M, p.(Ile247Met)) |
| ISCN |
- |
| DB-ID |
GJA8_000021 See all 6 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) |
0.00356 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2024-08-28 13:07:21 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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