NM_000546.6:c.215C>G

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  2. NM_000546.6:c.215C>G

HGVS Expressions

  • NG_017013.2:g.16397C>G
  • NM_000546.6:c.215C>G
  • NP_000537.3:p.Pro72Arg

Associated Genes

Tumor Protein p53
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Genomic Location

chr17:7676154

Clinvar Clinical Significance

Benign, Drug Response

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1042522

Clinvar

12351

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.27LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B21' from family 2 in the publi...
114480.28LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B22' from family 3 in the publi...
114480.29LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B23' from family 4 in the publi...
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Contributors

  • Asha Deepthi: 06.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 06.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.