Mutations

Reset Report

Report Settings

ToggleEditMutation = 'c.1309+34C>A'
ToggleEditBenign Mutations
ToggleEditAnimal Model

Mutation
2Benign Mutations, Animal Model

1 - 1 of 1

	PosAscending	Mutation	Protein	Primary	Exon/Intron	#Patients	#Alleles
	1309	c.1309+34C>A	(intronic)	Benign	Intron 10

1 - 1 of 1

c.1309+34C>A, (intronic)

The sequence variant c.1309+34C>A (dbSNP rs34324185) is located in intron 10. It has a minor allele frequency of 0.21-0.36 in different populations, and is considered a common, benign SNP.

Mutation Details

Mutation type

Benign

Localization

Intron 10

Number of Patients

References

Berg et al. 1999

Riise Stensland et al. 2012

Primary Mutation Type Distribution