Variant #0000603923 (NC_000011.9:g.5222877_5250289del, HBB(NM_000518.4):c.-2038_*23951del)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5222877_5250289del |
DNA change (hg38) |
g.5201647_5229059del |
Published as |
Vietnamese, SE Asian (HPFH-7, SEA-HPFH), NC_000011.10:g.5201647-5229059del27412bp |
ISCN |
- |
DB-ID |
HBB_004012 |
Variant remarks |
HPFH, Hb F levels |
Reference |
IthaNet-1505 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
IthaNet - Petros Kountouris |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
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