NM_000077.4:c.442G>A

HGVS Expressions

  • NG_007485.1:g.28575G>A
  • NM_000077.4:c.442G>A
  • NP_000068.1:p.Ala148Thr
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Genomic Location

chr9:21970917

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

3731249

Clinvar

41580

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.43LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B39' from family 16 in the publ...
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