NM_033226.2:c.490G>T

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HGVS Expressions

  • NM_033226.2:c.490G>T
  • NP_150229.2:p.Gly164Ter

Associated Genes

ATP-Binding Cassette, Subfamily C, Member 12
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Genomic Location

chr16:48140854

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

141807269

Clinvar

773580

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.34LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B28' from family 35 in the publ...
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Contributors

  • Asha Deepthi: 21.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 21.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.