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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-11-08 15:46:08 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 ?/. - c.220_221delinsTT Hb Meylan r.(?) p.(Asp74Phe)


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