Variant #0000324032 (NC_000015.9:g.42693952C>T, NM_000070.2:c.1468C>T (CAPN3))
| Chromosome |
15 |
| 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.42693952C>T |
| DNA change (hg38) |
g.42401754C>T |
| Published as |
CAPN3(NM_000070.2):c.1468C>T (p.(Arg490Trp)), CAPN3(NM_000070.3):c.1468C>T (p.R490W) |
| ISCN |
- |
| DB-ID |
CAPN3_000009 See all 82 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) |
9.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|