Variant #0000706220 (NC_000017.10:g.48267264C>A, NM_000088.3:c.2569G>T (COL1A1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48267264C>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL1A1_000164 See all 14 reported entries |
| Variant remarks |
- |
| Reference |
{PMID29499418 : Mrosk et al., 2018} |
| ClinVar ID |
- |
| dbSNP ID |
rs72653141 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Raymond Dalgleish |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Raymond Dalgleish |
| Date created |
2019-08-19 15:20:26 +02:00 (CEST) |
| Date last edited |
2022-05-13 16:34:57 +02:00 (CEST) |

Variant on transcripts
Screenings
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