NM_004260.3:c.3314G>A

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HGVS Expressions

  • NG_016430.1:g.10837G>A
  • NM_004260.3:c.3314G>A
  • NP_004251.3:p.Gly1105Asp

Associated Genes

RECQ Protein-Like 4
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Genomic Location

chr8:144511990

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

36078464

Clinvar

135151

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.40LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B36' from family 13 in the publ...
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Contributors

  • Asha Deepthi: 23.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 23.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.