NM_000038.6:c.6821C>T

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  2. NM_000038.6:c.6821C>T

HGVS Expressions

  • NG_008481.4:g.154895C>T
  • NM_000038.6:c.6821C>T
  • NP_000029.2:p.Ala2274Val

Associated Genes

APC Gene
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Genomic Location

chr5:112842415

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

34919187

Clinvar

41511

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.30LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B24' from family 5 in the publi...
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Contributors

  • Asha Deepthi: 13.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 13.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.