Variant #0000622158 (NC_000009.11:g.123769184G>A, NM_001735.2:c.2420C>T (C5))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.123769184G>A |
| DNA change (hg38) |
g.121006906G>A |
| Published as |
C5(NM_001317163.1):c.2438C>T (p.T813I), C5(NM_001735.2):c.2420C>T (p.T807I) |
| ISCN |
- |
| DB-ID |
C5_000021 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) |
0.00017 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|