Variant #0000473816 (NC_000017.10:g.76989790del, NM_001159772.1:c.1048del (CANT1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.76989790del |
| DNA change (hg38) |
g.78993708del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CANT1_000014 |
| Variant remarks |
Desbuquois Dysplasia |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs1294064847 |
| Origin |
Unknown |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Cynthia Silveira |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Cynthia Silveira |
| Date created |
2019-04-18 16:24:03 +02:00 (CEST) |
| Date last edited |
2021-09-09 14:41:03 +02:00 (CEST) |

Variant on transcripts
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