Full data view for gene HBB

Information The variants shown are described using the NM_000518.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 1 c.17del Hb Antalya r.(?) p.(Pro6Leufs*14) Parent #1 - VUS g.5248236del g.5227006del [16delC;8_9insC] - HBB_004082 - data from Globin Gene Server (HbVar-1135), OMIM:var0503, PubMed: Keser I. - - Germline - - - - - DNA SEQ, ? ?, screen APC gene (index patient), FAP1, thal - Japan, Tokyo, Department of Biochemistry, Cancer Institute - - - - - - - no (pedigree) - 1 Stefan Aretz
+/. - c.17del Hb Antalya r.(?) p.(Pro6Leufs*14) Unknown - pathogenic g.5248236del g.5227006del CD 3 (+T), CD 5 (-C) [Leu-Thr-Pro>Ser-Asp-Ser], [16delC;9_10insT] - HBB_004082 β-thalassaemia, β-chain variant, Haemolytic anaemia, Ineffective erythropoiesis IthaNet-53 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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