Thalassemias, beta
OMIM:613985Mode of inheritance:Autosomal dominant
Disease classification:Disorders involving the immune mechanism
Mutations
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.25_26delAA |
A.A. Change | p.Lys9ValfsX14 |
Exon/Intron | exon 1 |
Mutation Type | deletion |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.20delA |
A.A. Change | p.Glu7GlyfsX13 |
Exon/Intron | exon 1 |
Mutation Type | deletion |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.92+1G>A |
A.A. Change | |
Exon/Intron | intron 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.118C>T |
A.A. Change | p.Gln40X |
Exon/Intron | exon 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.-79A>G |
A.A. Change | |
Exon/Intron | 5' of the ATG codon |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.-151C>T |
A.A. Change | |
Exon/Intron | 5' of the ATG codon |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.-78A>G |
A.A. Change | |
Exon/Intron | 5' of the ATG codon |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.92+2T>C |
A.A. Change | |
Exon/Intron | intron 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.92+6T>C |
A.A. Change | |
Exon/Intron | intron 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.93-21G>A |
A.A. Change | |
Exon/Intron | intron 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.93-1G>A |
A.A. Change | |
Exon/Intron | intron 1 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
DNA Change | 25bp deletion |
A.A. Change | |
Exon/Intron | exon 1 |
Mutation Type | deletion |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.114G>A |
A.A. Change | p.Trp38X |
Exon/Intron | exon 2 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.315+1G>A |
A.A. Change | |
Exon/Intron | intron 2 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.-240G>A |
A.A. Change | |
Exon/Intron | 5' of the ATG codon |
Mutation Type | substitution |
Reference | Agouti I, Badens C, Abouyoub A, Levy N, Bennani M.Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity. Genet Test. 2008 Dec;12(4):563-8. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.316-125A>G |
A.A. Change | |
Exon/Intron | intron 2 |
Mutation Type | substitution |
Reference | Agouti I, Badens C, Abouyoub A, Levy N, Bennani M.Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity. Genet Test. 2008 Dec;12(4):563-8. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.-31C>T |
A.A. Change | |
Exon/Intron | 5' of the ATG codon |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
Gene Symbol | HBB |
---|---|
Reference transcript | NM_000518.4 |
DNA Change | c.316-106C>G |
A.A. Change | |
Exon/Intron | intron 2 |
Mutation Type | substitution |
Reference | Lemsaddek W, Picanco I, Seuanes F, Nogueira P, Mahmal L, Benchekroun S, Khattab M, Osorio-Almeida L.The beta-thalassemia mutation/haplotype distribution in the moroccan population. Hemoglobin. 2004 Feb;28(1):25-37. |
  Variant not named according to HGVS recommendations