Variant #0000876070 (NC_000017.10:g.(48265511_48265890)_(48279000_?)dup, NM_000088.3:c.-126_(3207+1_3208-1){2} (COL1A1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(48265511_48265890)_(48279000_?)dup |
| DNA change (hg38) |
g.(50188150_50188529)_(50201639_?)dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL1A1_001137 See all 2 reported entries |
| Variant remarks |
multi-exon deletion encompassing exon 1; haploinsufficiency is a known dominant pathogenic mechanism in COL1A1 |
| 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
|