NM_017791.3:c.1276G>A - CAGS

NM_017791.3:c.1276G>A

HGVS Expressions

NG_027694.1:g.67399G>A
NM_017791.3:c.1276G>A
NP_060261.2:p.Ala426Thr
NC_000014.9:g.75640995G>A

Associated Genes

FLVCR Heme Transporter 2

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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

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Subject ID	Country of Origin	Allele Count	CTGA Clinical Significance	Condition(s)	Reference	Remarks
225790.1	Saudi Arabia	2	Uncertain Significance	Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome	Monies et al. 2017

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Contributors

Asha Deepthi: 17.03.2025

Edit History

Asha Deepthi: 17.03.2025

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© CAGS 2025. All rights reserved.

© CAGS 2025. All rights reserved.