Variant #0000001173 (NC_000012.11:g.21968761C>T, ABCC9(NM_020297.2):c.3959G>A)
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21968761C>T |
Reference |
GenBank |
DB-ID |
ABCC9_000015 |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
- |
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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