NM_001352514.2:c.865G>A - CAGS

NM_001352514.2:c.865G>A

HGVS Expressions

NG_016193.2:g.58374G>A
NM_001352514.2:c.865G>A
NP_001339443.1:p.Val289Ile
NC_000021.9:g.36937021C>T

Associated Genes

Holocarboxylase Synthetase

Back to search Result

Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

Show entries

Search:

Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Reference	Remarks
609018.G.5	Qatar	451	0.0161	Likely Benign	Devadoss Gandhi et al. 2024	451 individuals from a study of 14,060 Q...
609018.G.6	Qatar	24	0.0161	Likely Benign	Devadoss Gandhi et al. 2024	12 individuals from a study of 14,060 Qa...

Download Table

Contributors

Sayeeda Hana: 14.03.2025

Edit History

Sayeeda Hana: 14.03.2025

Back to search Result

© CAGS 2025. All rights reserved.

© CAGS 2025. All rights reserved.