NM_001363711.1:c.3082_3085delinsGCTTCCT

HGVS Expressions

  • NG_009447.1:g.19010_19013delinsGCTTCCT
  • NM_001363711.1:c.3082_3085delinsGCTTCCT
  • NP_001350640.1:p.Leu1028delinsAlaSerTer
  • NC_000015.10:g.45100149_45100152delinsAGGAAGC

Associated Genes

Dual Oxidase 2
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CTGA Clinical Significance

Pathogenic

Variant Type

Indel

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607200.1.1Oman2PathogenicThyroid Dyshormonogenesis 6Nicholas et al. 2016
607200.1.2Oman1Nicholas et al. 2016
607200.1.3Oman1Nicholas et al. 2016
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