Variant #0000603265 (NC_000011.9:g.5248158A>G, NC_000011.9(NM_000518.4):c.92+2T>C (HBB))
| 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.5248158A>G |
| DNA change (hg38) |
g.5226928A>G |
| Published as |
IVS I-2 (T>C) |
| ISCN |
- |
| DB-ID |
HBB_001140 See all 13 reported entries |
| Variant remarks |
β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis |
| Reference |
IthaNet-105 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
IthaNet - Petros Kountouris |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-11-08 15:46:08 +01:00 (CET) |
| Date last edited |
2020-06-29 18:06:44 +02:00 (CEST) |

Variant on transcripts
|