NM_004972.3:c.1597A>T

HGVS Expressions

  • NG_009904.1:g.89764A>T
  • NM_004972.3:c.1597A>T
  • NP_004963.1:p.Asn533Tyr

Associated Genes

Janus Kinase 2
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Genomic Location

chr9:5070008

Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
208900.1Lebanon1Likely PathogenicLeukemia, Acute MyeloidNair et al. 2018
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