NM_000546.6:c.245C>T

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HGVS Expressions

  • NG_017013.2:g.16427C>T
  • NM_000546.6:c.245C>T
  • NP_000537.3:p.Pro82Leu

Associated Genes

Tumor Protein p53
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Genomic Location

chr17:7676124

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

dbSNP

534447939

Clinvar

182946

Epidemiology in the Arab World

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Contributors

  • Asha Deepthi: 02.09.2020

Edit History

  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 02.09.2020
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.