NM_001048174.2:c.1174C>A

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  2. NM_001048174.2:c.1174C>A

HGVS Expressions

  • NG_008189.1:g.13986C>A
  • NM_001048174.2:c.1174C>A
  • NP_001041639.1:p.Leu392Met

Associated Genes

MutY DNA Glycosylase
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Genomic Location

chr1:45331485

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

144079536

Clinvar

41752

Epidemiology in the Arab World

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

  • Asha Deepthi: 29.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 29.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.