Variant #0000874934 (NC_000017.10:g.48277320_48277321delinsTT, NC_000017.10(NM_000088.3):c.104-13_104-12delinsAA (COL1A1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48277320_48277321delinsTT |
| DNA change (hg38) |
g.50199959_50199960delinsTT |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL1A1_000937 See all 2 reported entries |
| Variant remarks |
Loss of splice acceptor site predicted |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Gerard Pals |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-08-13 13:51:05 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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