Variant #0000000248 (NC_000011.9:g.5255757G>A, HBD(NM_000519.3):c.-94G>A)
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5255757G>A |
Reference |
Xiong et al |
DB-ID |
HBD_000032 |
Frequency |
- |
Variant remarks |
-44 G>A |
ClassClinical |
Pathogenic |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |
Variant on transcripts
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