Variant #0000000168 (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 |
100/238 |
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
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