Variant #0000000162 (NC_000006.11:g.135447773T>C, MYB(NM_001130173.1):c.-54879T>C)
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.135447773T>C |
Reference |
C-C So,et al;dbSNP |
DB-ID |
MYB_000006 |
Frequency |
134/238 |
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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