Variant #0000058486 (NC_000004.11:g.109971415T>A, NC_000004.11(NM_198721.2):c.368-80A>T (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.109971415T>A |
| DNA change (hg38) |
g.109050259T>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
COL25A1_000006 |
| Variant remarks |
Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message. |
| Reference |
PubMed: Shinwari 2015, Journal: Shinwari 2015 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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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