NM_020975.6:c.2508C>T

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HGVS Expressions

  • NG_007489.1:g.47578C>T
  • NM_020975.6:c.2508C>T
  • NP_066124.1:p.Ser836=

Associated Genes

Rearranged during Transfection Protooncogene
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Genomic Location

chr10:43119646

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1800862

Clinvar

24946

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.46LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B42' from family 19 in the publ...
114480.49LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B45' from family 22 in the publ...
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Contributors

  • Asha Deepthi: 27.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 27.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.