Variant #0000002695 (NC_000003.12:g.27541G>A, NM_000094.4:c.6860G>A (COL7A1))
Individual ID |
00000610 |
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.27541G>A |
Published as |
- |
Reference |
M M Tang et al.(2013) |
DB-ID |
COL7A1_000001 |
dbSNP ID |
rs1800061 |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nur Aisyah Athirah |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nur Aisyah Athirah |
Date created |
2021-05-04 09:27:08 +08:00 (CST) |
Date last edited |
2021-09-08 13:04:33 +08:00 (CST) |

Variant on transcripts
Screenings
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