Variant #0000001245 (NC_000004.12:g.4862963C>A, NM_002448.3:c.732C>A (MSX1))
Individual ID |
00000246 |
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.4862963C>A |
Published as |
c.732G>A |
Reference |
- |
DB-ID |
MSX1_000003 See all 3 reported entries |
dbSNP ID |
rs779274456 |
Frequency |
1 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-12-13 14:20:37 +08:00 (CST) |
Date last edited |
2021-09-08 12:44:34 +08:00 (CST) |

Variant on transcripts
Screenings
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