NM_000771.3:c.449G>C

HGVS Expressions

  • NG_008385.1:g.8652G>C
  • NM_000771.3:c.449G>C
  • NP_000762.2:p.Arg150Pro
  • NC_000010.11:g.94942309G>C
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Variant Type

Substitution

dbSNP

7900194

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
171050.G.1United Arab Emirates0.02Al-Mahayri et al. 2020 100 (52 females, 48 males) normal health...
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