NM_001171.5:c.3803G>A

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HGVS Expressions

  • NG_007558.2:g.70730G>A
  • NM_001171.5:c.3803G>A
  • NP_001162.4:p.Arg1268Gln
  • NC_000016.10:g.16157742C>T

Associated Genes

ATP-Binding Cassette, Subfamily C, Member 6
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Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

2238472

Clinvar

6570

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.5LebanonDrug ResponseBreast CancerAwada et al. 2013 Case-control study observed 12 SNPs to b...
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Contributors

  • Asha Deepthi: 20.01.2021

Edit History

  • Asha Deepthi: 21.01.2021
  • Asha Deepthi: 20.01.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.