Variant #0000001217 (NC_000015.9:g.35082659T>C, ACTC1(NM_005159.4):c.1088A>G)
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35082659T>C |
Reference |
GenBank |
DB-ID |
ACTC1_000021 |
Frequency |
0.2 |
Variant remarks |
Exon |
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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