NM_002458.2:c.10352C>T

HGVS Expressions

  • NG_031880.1:g.29168C>T
  • NM_002458.2:c.10352C>T
  • NP_002449.2:p.Thr3451Met
  • NC_000011.10:g.1247232C>T
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613990.1United Arab Emirates1Likely PathogenicInterstitial Lung Disease 2Alsamri et al. 2020; Alsamri et al. 2021 Authors mention that variant 10352C>T ma...
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