Variant #0000000188 (NC_000006.11:g.135426558A>T, HBS1L(NM_006620.3):c.-50729T>A)
Chromosome |
6 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135426558A>T |
Reference |
C-C So,et al;dbSNP |
DB-ID |
HBS1L_000004 See all 3 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
|
|