NM_001077490.3:c.1046C>T

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  2. NM_001077490.3:c.1046C>T

HGVS Expressions

  • NG_016194.2:g.19759C>T
  • NM_001077490.3:c.1046C>T
  • NP_001070958.1:p.Pro349Leu

Associated Genes

GNAS Complex Locus
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Genomic Location

chr20:58854498

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

373809205

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.52LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B48' from family 38 in the publ...
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Contributors

  • Asha Deepthi: 28.09.2020

Edit History

  • Sayeeda Hana: 08.06.2021
  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 28.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.