NM_001082.5:c.1297G>A

HGVS Expressions

  • NG_007971.2:g.23454G>A
  • NM_001082.5:c.1297G>A
  • NP_001073.3:p.Val433Met
  • NC_000019.10:g.15879621C>T
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Clinvar Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

2108622

Clinvar

225969

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
171050.G.1United Arab Emirates0.4592Al-Mahayri et al. 2020 100 (52 females, 48 males) normal health...
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