NM_007294.4:c.4654T>C

  1. Home
  2. NM_007294.4:c.4654T>C

HGVS Expressions

  • NG_005905.2:g.143632T>C
  • NM_007294.4:c.4654T>C
  • NP_009225.1:p.Tyr1552His

Associated Genes

Breast Cancer 1 Gene
Back to search Result
Genomic Location

chr17:43074352

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

1265352633

Clinvar

433716

Epidemiology in the Arab World

View Map
Download Table

Contributors

  • Asha Deepthi: 03.06.2020

Edit History

  • Asha Deepthi: 07.06.2020
  • Asha Deepthi: 03.06.2020
Back to search Result
© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.