Variant #0000603495 (NC_000011.9:g.5248195_5248200del, NM_000518.4:c.54_59del (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.5248195_5248200del |
DNA change (hg38) |
g.5226965_5226970del |
Published as |
CD 17/18 (-AAGGTG), 52_57delAAGGTG |
ISCN |
- |
DB-ID |
HBB_001058 See all 2 reported entries |
Variant remarks |
β-chain variant |
Reference |
IthaNet-855 |
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 |
2020-06-29 18:09:44 +02:00 (CEST) |

Variant on transcripts
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