NM_000369.5:c.1295A>G

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HGVS Expressions

  • NG_009206.1:g.192829A>G
  • NM_000369.5:c.1295A>G
  • NP_000360.2:p.Asn432Ser
  • NC_000014.9:g.81143353A>G

Associated Genes

Thyroid-Stimulating Hormone Receptor
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

368268514

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
603372.1United Arab Emirates2NAUncertain SignificanceMahfouz et al. 2020
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Contributors

  • Asha Deepthi: 12.07.2022

Edit History

  • Asha Deepthi: 12.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.