NM_000535.7:c.1688G>T

HGVS Expressions

  • NG_008466.1:g.27030G>T
  • NM_000535.7:c.1688G>T
  • NP_000526.2:p.Arg563Leu
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Genomic Location

chr7:5987077

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

41705

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.44LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B40' from family 17 in the publ...
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