NM_001083602.2:c.4126C>T

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  2. NM_001083602.2:c.4126C>T

HGVS Expressions

  • NG_007664.1:g.75034C>T
  • NM_001083602.2:c.4126C>T
  • NP_001077071.1:p.Arg1376Trp

Associated Genes

Patched 1
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Genomic Location

chr9:95446932

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

143464326

Clinvar

41666

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.42LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B38' from family 15 in the publ...
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Contributors

  • Asha Deepthi: 08.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 08.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.