NM_000059.4:c.7242A>G

HGVS Expressions

  • NG_012772.3:g.44616A>G
  • NM_000059.4:c.7242A>G
  • NP_000050.3:p.Ser2414=

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32355095

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799955

Clinvar

126133

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.38LebanonBenignBreast CancerJalkh et al, 2012 13 unrelated patients with breast cancer
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