NM_000546.6:c.245C>T

  1. Home
  2. NM_000546.6:c.245C>T

HGVS Expressions

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

Associated Genes

Tumor Protein p53
Back to search Result
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

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.29LebanonPathogenicBreast CancerJalkh et al, 2017 Patient 'B23' from family 4 in the publi...
Download Table

Contributors

  • Asha Deepthi: 02.09.2020

Edit History

  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 02.09.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.