Variant #0000328592 (NC_000020.10:g.61450653C>T, NC_000020.10(NM_001853.3):c.255+8C>T (COL9A3))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.61450653C>T |
| DNA change (hg38) |
g.62819301C>T |
| Published as |
COL9A3(NM_001853.3):c.255+8C>T (p.(=)), COL9A3(NM_001853.4):c.255+8C>T |
| ISCN |
- |
| DB-ID |
COL9A3_000079 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00097 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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