ABO > ABO*O.01.41
Allele Information
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Phenotypes
A
B
A,B
A1
Genetic Changes
nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
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c.261delG | p.Thr88Profs*31 | Exon 6 | chr9:136,132,909 | chr9:133,257,493 |
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c.297A>G | Exon 6 | chr9:136,132,873 | chr9:133,257,457 |
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c.526C>G | p.Arg176Gly | Exon 7 | chr9:136,131,592 | chr9:133,256,176 |
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c.657C>T | Exon 7 | chr9:136,131,461 | chr9:133,256,045 |
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c.703G>A | p.Gly235Ser | Exon 7 | chr9:136,131,415 | chr9:133,255,999 |
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c.796C>A | p.Leu266Met | Exon 7 | chr9:136,131,322 | chr9:133,255,906 |
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c.803G>C | p.Gly268Ala | Exon 7 | chr9:136,131,315 | chr9:133,255,899 |
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c.930G>A | Exon 7 | chr9:136,131,188 | chr9:133,255,772 |
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Sequence
None
Publication
None