Variant #0000604042 (NC_000011.9:g.5247901_5247902delinsAA, NM_000518.4:c.220_221delinsTT (HBB))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5247901_5247902delinsAA |
| DNA change (hg38) |
g.5226671_5226672delinsAA |
| Published as |
CD 73 GAT>TAT>TTT [Asp>Phe], [220G>T;221A>T] |
| ISCN |
- |
| DB-ID |
HBB_004163 |
| Variant remarks |
β-chain variant |
| Reference |
IthaNet-2478 |
| 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 |
| Date created |
2019-11-08 15:46:08 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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