Variant #0000324026 (NC_000015.9:g.42681133G>A, NM_000070.2:c.640G>A (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.42681133G>A |
| DNA change (hg38) |
g.42388935G>A |
| Published as |
CAPN3(NM_000070.2):c.640G>A (p.G214S, p.(Gly214Ser)), CAPN3(NM_000070.3):c.640G>A (p.G214S) |
| ISCN |
- |
| DB-ID |
CAPN3_000074 See all 19 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 |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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