Variant #0000912452 (NC_000006.11:g.31915564T>C, NM_006929.4:c.-11406T>C (SKIV2L))
| Chromosome |
6 |
| 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.31915564T>C |
| DNA change (hg38) |
- |
| Published as |
CFB(NM_001710.5):c.704T>C (p.L235P) |
| ISCN |
- |
| DB-ID |
C2_000061 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-01-11 15:44:22 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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