NM_000546.6:c.673-36G>C - CAGS

NM_000546.6:c.673-36G>C

HGVS Expressions

NG_017013.2:g.18225G>C
NM_000546.6:c.673-36G>C

Associated Genes

Tumor Protein p53

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Genomic Location

chr17:7674326

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

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Subject ID	Country of Origin	CTGA Clinical Significance	Condition(s)	Reference	Remarks
114480.47	Lebanon	Association	Breast Cancer	Jalkh et al, 2017	Patient 'B43' from family 20 in the publ...
114480.54	Lebanon	Association	Breast Cancer	Jalkh et al, 2017	Patient 'B50' from family 25 in the publ...

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Contributors

Asha Deepthi: 02.09.2020

Edit History

Asha Deepthi: 05.10.2020
Asha Deepthi: 02.09.2020

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© CAGS 2025. All rights reserved.

© CAGS 2025. All rights reserved.