NM_032444.4:c.5501A>G

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  2. NM_032444.4:c.5501A>G

HGVS Expressions

  • NG_028123.1:g.34239A>G
  • NM_032444.4:c.5501A>G
  • NP_115820.2:p.Asn1834Ser

Associated Genes

SLX4 Structure-Specific Endonuclease Subunit
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Genomic Location

chr16:3582346

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

111738042

Clinvar

241697

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.51LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B47' from family 37 in the publ...
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Contributors

  • Asha Deepthi: 07.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 07.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.