Variant #0000866290 (NC_000019.9:g.6718128G>A, NM_000064.2:c.481C>T (C3))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6718128G>A |
| DNA change (hg38) |
- |
| Published as |
C3(NM_000064.2):c.481C>T (p.R161W) |
| ISCN |
- |
| DB-ID |
C3_000047 See all 2 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 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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