Variant #0000000169 (NC_000006.11:g.135455329A>G, MYB(NM_001130173.1):c.-47323A>G)
| Chromosome |
6 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135455329A>G |
| Reference |
C-C So,et al;dbSNP |
| DB-ID |
MYB_000009 See all 2 reported entries |
| Frequency |
133/238 |
| Variant remarks |
- |
| ClassClinical |
Likely benign |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |

Variant on transcripts
|
|