Variant #0000874935 (NC_000017.10:g.48277311G>C, NC_000017.10(NM_000088.3):c.104-3C>G (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.48277311G>C |
DNA change (hg38) |
g.50199950G>C |
Published as |
- |
ISCN |
- |
DB-ID |
COL1A1_000142 See all 2 reported entries |
Variant remarks |
Loss of splice acceptor site predicted |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs72667009 |
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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