NM_007294.4:c.4308T>C

HGVS Expressions

  • NG_005905.2:g.135531T>C
  • NM_007294.4:c.4308T>C
  • NP_009225.1:p.Ser1436=

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43082453

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1060915

Clinvar

125703

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.19LebanonBenignBreast CancerJalkh et al, 2012 44 unrelated patients with breast cancer
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