NM_024685.4:c.1365T>G

HGVS Expressions

  • NG_016357.1:g.6823T>G
  • NM_024685.4:c.1365T>G
  • NP_078961.3:p.Tyr455Ter
  • NC_000012.12:g.76346620A>C

Associated Genes

BBS10 Gene
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

1029918

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615987.4Saudi Arabia2PathogenicBardet-Biedl Syndrome 10Abu-Safieh et al. 2012 "BBS-F011-A" in the publication
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