Variant #0000874921 (NC_000017.10:g.48278808G>A, NM_000088.3:c.67C>T (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.48278808G>A |
DNA change (hg38) |
g.50201447G>A |
Published as |
- |
ISCN |
- |
DB-ID |
COL1A1_001424 See all 2 reported entries |
Variant remarks |
Nonsense variants are a known 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
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