NM_002524.5:c.181C>A - CAGS

NM_002524.5:c.181C>A

HGVS Expressions

NG_007572.1:g.7986C>A
NM_002524.5:c.181C>A
NP_002515.1:p.Gln61Lys
NC_000001.11:g.114713909G>T

Associated Genes

NRAS Protooncogene, GTPase

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Clinvar Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic, Uncertain Significance

CTGA Clinical Significance

Likely Pathogenic

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
188550.G.1	Lebanon			Likely Pathogenic	Thyroid Carcinoma, Papillary	Fakhruddin et al. 2017	253 cases of PTC

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Contributors

Pratibha Nair: 09.05.2021

Edit History

Pratibha Nair: 09.05.2021

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© CAGS 2024. All rights reserved.

© CAGS 2024. All rights reserved.