NM_005591.4:c.1728A>T

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HGVS Expressions

  • NG_007261.1:g.51601A>T
  • NM_005591.4:c.1728A>T
  • NP_005582.1:p.Arg576=

Associated Genes

MRE11 Homolog, Double Strand Break Repair Nuclease
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Genomic Location

chr11:94447274

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

876658330

Clinvar

230008

Epidemiology in the Arab World

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Contributors

  • Asha Deepthi: 08.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 08.09.2020
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.