NM_000455.5:c.1211C>T

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  2. NM_000455.5:c.1211C>T

HGVS Expressions

  • NG_007460.2:g.42150C>T
  • NM_000455.5:c.1211C>T
  • NP_000446.1:p.Ser404Phe

Associated Genes

Serine/Threonine Protein Kinase 11
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Genomic Location

chr19:1226556

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

200078204

Clinvar

127700

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.40LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B36' from family 13 in the publ...
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Contributors

  • Asha Deepthi: 14.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 14.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.