NM_000583.4:c.1307C>A

HGVS Expressions

  • NG_012837.3:g.57915C>A
  • NM_000583.4:c.1307C>A
  • NP_000574.2:p.Thr436Lys
  • NC_000004.12:g.71752606G>T

Associated Genes

Group-Specific Component
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Clinical Significance

Benign

Variant Type

Substitution

dbSNP

4588

Clinvar

15986

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
139200.G.1LebanonAssociation,Uncertain SignificanceMedlej-Hashim et al. 2015 Study subjects with GG genotype of rs704...
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