NM_000388.3:c.1861G>A

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  2. NM_000388.3:c.1861G>A

HGVS Expressions

  • NG_009058.1:g.105133G>A
  • NM_000388.3:c.1861G>A
  • NP_000379.2:p.Val621Met
  • NC_000003.12:g.122283815G>A

Associated Genes

Calcium-Sensing Receptor
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

751538967

Clinvar

660430

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
178500.2.1United Arab Emirates1Uncertain SignificanceAlsamri et al. 2020; Alsamri et al. 2021
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Contributors

  • Pratibha Nair: 24.02.2022

Edit History

  • Pratibha Nair: 24.02.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.