NM_005591.4:c.1491C>T

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  2. NM_005591.4:c.1491C>T

HGVS Expressions

  • NG_007261.1:g.39458C>T
  • NM_005591.4:c.1491C>T
  • NP_005582.1:p.Ile497=

Associated Genes

MRE11 Homolog, Double Strand Break Repair Nuclease
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Genomic Location

chr11:94459417

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

199634245

Clinvar

184438

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.28LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B22' from family 3 in the publi...
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Contributors

  • Asha Deepthi: 08.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 08.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.