NM_007294.4:c.1456T>C - CAGS

NM_007294.4:c.1456T>C

HGVS Expressions

NG_005905.2:g.123909T>C
NM_007294.4:c.1456T>C
NP_009225.1:p.Phe486Leu

Associated Genes

Breast Cancer 1 Gene

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Genomic Location

chr17:43094075

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

Lebanon

Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Condition(s)	Reference	Remarks
114480.G.1.3	Lebanon			Benign	Breast Cancer	Jalkh et al, 2012	2 unrelated patients with breast cancer

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Contributors

Asha Deepthi: 03.06.2020

Edit History

Asha Deepthi: 07.06.2020
Asha Deepthi: 03.06.2020

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© CAGS 2024. All rights reserved.

© CAGS 2024. All rights reserved.