Variant #0000922212 (NC_000010.10:g.101824970G>A, NM_001308.2:c.734C>T (CPN1))
| Chromosome |
10 |
| Allele |
Parent #2 |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.101824970G>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CPN1_000010 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
Journal: Vincent 2024 |
| ClinVar ID |
- |
| dbSNP ID |
rs371070915 |
| Origin |
CLASSIFICATION record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
8.0E-5 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2023-03-31 11:22:01 +02:00 (CEST) |
| Date last edited |
2024-02-12 08:42:58 +01:00 (CET) |

Variant on transcripts
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