NM_001128425.2:c.1258C>G

HGVS Expressions

  • NG_008189.1:g.13986C>G
  • NM_001128425.2:c.1258C>G
  • NP_001121897.1:p.Leu420Val

Associated Genes

MutY DNA Glycosylase
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Genomic Location

chr1:45331485

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

220923

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.26LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B19' from family 1 in the publi...
114480.32LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B26' from family 7 in the publi...
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