NM_032043.3:c.3571A>G

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HGVS Expressions

  • NG_007409.2:g.185085A>G
  • NM_032043.3:c.3571A>G
  • NP_114432.2:p.Ile1191Val

Associated Genes

BRCA1-Interacting Protein
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Genomic Location

chr17:61683475

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

761405340

Clinvar

186989

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.37LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B33' from family 10 in the publ...
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Contributors

  • Asha Deepthi: 21.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 21.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.