NM_020184.3:c.1813C>T

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HGVS Expressions

  • NG_016608.1:g.43287C>T
  • NM_020184.3:c.1813C>T
  • NP_064569.3:p.Arg605Ter
  • NC_000002.12:g.96799188C>T

Associated Genes

Cyclin M4
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1021713187

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
217080.G.2Palestine6NAUncertain SignificanceJalili SyndromeParry et al. 2009 3 patients from family 'Gaza B' in the p...
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Contributors

    Edit History

    • Asha Deepthi: 14.03.2021
    • Asha Deepthi: 05.02.2019
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    © CAGS 2024. All rights reserved.