NM_024649.5:c.889C>T

HGVS Expressions

  • NG_009093.1:g.17867C>T
  • NM_024649.5:c.889C>T
  • NP_078925.3:p.Arg297Trp
  • NC_000011.10:g.66523514C>T

Associated Genes

BBS1 Gene
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Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615989.3United Arab Emirates1Abu-Safieh et al. 2012 "BBS-F028-A" in the publication
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