NM_000129.4:c.103G>T

HGVS Expressions

  • NG_008107.1:g.7130G>T
  • NM_000129.4:c.103G>T
  • NP_000120.2:p.Val35Leu
  • NC_000006.12:g.6318562C>A

Associated Genes

Factor XIII, A1 Subunit
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Clinvar Clinical Significance

Benign, Uncertain Significance

CTGA Clinical Significance

Benign, Uncertain Significance

Variant Type

Substitution

dbSNP

5985

Clinvar

16532

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601367.3Lebanon2Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.5Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.6Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.23Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with arterial lesion
601367.29Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with small vessel lesion
601367.30Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with small vessel lesion
134570.G.1Lebanon304BenignMahfouz et al, 2008 Group of 152 healthy Lebanese individual...
134570.G.2Lebanon46BenignMahfouz et al, 2008 Group of 46 healthy Lebanese individuals...
134570.G.3Lebanon140.14BenignMahfouz et al, 2008 Group of 7 healthy Lebanese individuals ...
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