NM_001085377.2:c.152G>T

  1. Home
  2. NM_001085377.2:c.152G>T

HGVS Expressions

  • NG_012265.1:g.5568G>T
  • NM_001085377.2:c.152G>T
  • NP_001078846.2:p.Gly51Val

Associated Genes

Mutated in Colorectal Cancers
Back to search Result
Genomic Location

chr5:113488263

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.34LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B28' from family 35 in the publ...
Download Table

Contributors

  • Asha Deepthi: 21.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 21.09.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.