Variant #0000604178 (NC_000011.9:g.5246875T>G, HBB(NM_000518.4):c.399A>C)
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.5246875T>G |
DNA change (hg38) |
g.5225645T>G |
Published as |
CD 6 GAG>GTG, [20A>T;399A>C] |
ISCN |
- |
DB-ID |
HBB_000991 See all 5 reported entries |
Variant remarks |
β-chain variant Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. |
Reference |
IthaNet-814 |
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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