NM_000546.6:c.673-36G>C

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  2. NM_000546.6:c.673-36G>C

HGVS Expressions

  • NG_017013.2:g.18225G>C
  • NM_000546.6:c.673-36G>C

Associated Genes

Tumor Protein p53
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Genomic Location

chr17:7674326

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

17880604

Clinvar

221184

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.47LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B43' from family 20 in the publ...
114480.54LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B50' from family 25 in the publ...
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Contributors

  • Asha Deepthi: 02.09.2020

Edit History

  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 02.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.