Variant #0000058520 (NC_000004.11:g.109745336T>G, NM_198721.2:c.1839A>C (COL25A1))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.109745336T>G |
| DNA change (hg38) |
g.108824180T>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL25A1_000038 |
| Variant remarks |
- |
| Reference |
PubMed: Shinwari 2015, Journal: Shinwari 2015 |
| ClinVar ID |
- |
| dbSNP ID |
rs7689008 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.32225 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-02-14 19:25:50 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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