NM_000051.4:c.2572T>C

HGVS Expressions

  • NG_009830.1:g.49445T>C
  • NM_000051.4:c.2572T>C
  • NP_000042.3:p.Phe858Leu
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Genomic Location

chr11:108267276

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

1800056

Clinvar

132736

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.27LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B21' from family 2 in the publi...
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