NM_001085377.2:c.152G>T

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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
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Genomic Location

chr5:113488263

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Contributors

  • Asha Deepthi: 21.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 21.09.2020
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.