Variant #0000578417 (NC_000020.10:g.61468571T>C, NM_001853.3:c.1740T>C (COL9A3))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.61468571T>C |
| DNA change (hg38) |
g.62837219T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL9A3_000011 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Asamura 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
45/300 controls |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.68093 View details |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2011-10-21 16:34:54 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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