Variant #0000000172 (NC_000006.11:g.135411228T>C, HBS1L(NM_006620.3):c.-35399A>G)
| 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.135411228T>C |
| Reference |
Lai Y,et al;dbSNP |
| DB-ID |
HBS1L_000022 |
| Frequency |
89/238 |
| 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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