Variant #0001025579 (NC_000009.11:g.123751971G>A, NM_001735.2:c.3029C>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.123751971G>A |
| DNA change (hg38) |
- |
| Published as |
C5(NM_001317163.1):c.3047C>T (p.A1016V), C5(NM_001735.2):c.3029C>T (p.A1010V), C5(NM_001735.3):c.3029C>T (p.A1010V) |
| ISCN |
- |
| DB-ID |
C5_000005 See all 4 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) |
0.00067 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2025-02-07 18:57:27 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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