NM_024675.4:c.2993G>A

HGVS Expressions

  • NG_007406.1:g.23386G>A
  • NM_024675.4:c.2993G>A
  • NP_078951.2:p.Gly998Glu
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Genomic Location

chr16:23622972

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

Clinvar

126699

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.40LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B36' from family 13 in the publ...
114480.47LebanonAssociationBreast CancerJalkh et al, 2017 Patient 'B43' from family 20 in the publ...
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