NM_007294.4:c.3526G>A

HGVS Expressions

  • NG_005905.2:g.125979G>A
  • NM_007294.4:c.3526G>A
  • NP_009225.1:p.Val1176Ile

Associated Genes

Breast Cancer 1 Gene
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Genomic Location

chr17:43092005

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

565640

Epidemiology in the Arab World

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