Variant #0000000200 (NC_000006.11:g.135324165A>C, HBS1L(NM_006620.3):c.431-185T>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.135324165A>C |
Reference |
Yi S,et al;dbSNP |
DB-ID |
HBS1L_000008 |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
uncertain significance |
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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