NM_022455.5:c.2224_2243del

HGVS Expressions

  • NG_009821.1:g.82545_82564del
  • NM_022455.5:c.2224_2243del
  • NP_071900.2:p.Pro742Ter
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Genomic Location

chr5:177210623-177210642

CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.37LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B33' from family 10 in the publ...
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