Variant #0000000191 (NC_000006.11:g.135427159T>C, HBS1L(NM_006620.3):c.-51330A>G)
Chromosome |
6 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135427159T>C |
Reference |
Yunyan He,et al ;dbSNP |
DB-ID |
HBS1L_000026 |
Frequency |
16/312 |
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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