Variant #0000603259 (NC_000011.9:g.5248160C>T, HBB(NM_000518.4):c.92G>A)
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.5248160C>T |
DNA change (hg38) |
g.5226930C>T |
Published as |
CD 30 (G>A) or IVS I (-1) AGG>AAG (Arg>Lys) |
ISCN |
- |
DB-ID |
HBB_001136 See all 2 reported entries |
Variant remarks |
β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis |
Reference |
IthaNet-99 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
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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