NM_000546.6:c.215C>G - CAGS

NM_000546.6:c.215C>G

HGVS Expressions

NG_017013.2:g.16397C>G
NM_000546.6:c.215C>G
NP_000537.3:p.Pro72Arg

Associated Genes

Tumor Protein p53

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Genomic Location

chr17:7676154

Clinvar Clinical Significance

Benign, Drug Response

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

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Search:

Subject ID	Country of Origin	CTGA Clinical Significance	Condition(s)	Reference	Remarks
114480.27	Lebanon	Uncertain Significance	Breast Cancer	Jalkh et al, 2017	Patient 'B21' from family 2 in the publi...
114480.28	Lebanon	Uncertain Significance	Breast Cancer	Jalkh et al, 2017	Patient 'B22' from family 3 in the publi...
114480.29	Lebanon	Uncertain Significance	Breast Cancer	Jalkh et al, 2017	Patient 'B23' from family 4 in the publi...

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Contributors

Asha Deepthi: 06.09.2020

Edit History

Asha Deepthi: 26.01.2021
Asha Deepthi: 30.09.2020
Asha Deepthi: 06.09.2020

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© CAGS 2025. All rights reserved.

© CAGS 2025. All rights reserved.