NM_001211.6:c.1535A>G

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  2. NM_001211.6:c.1535A>G

HGVS Expressions

  • NG_016338.1:g.44940A>G
  • NM_001211.6:c.1535A>G
  • NP_001202.5:p.Glu512Gly

Associated Genes

BUB1 Mitotic checkpoint Serine/Threonine Kinase B
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Genomic Location

chr15:40200948

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

747225593

Clinvar

1061723

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.58LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'D6' from family 29 in the publi...
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Contributors

  • Asha Deepthi: 29.09.2020

Edit History

  • Sami Bizzari: 06.06.2021
  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 29.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.