Mutations

Reset Report

Report Settings

ToggleEditMutation = 'c.2268-45T>G'
ToggleEditBenign Mutations
ToggleEditAnimal Model

Mutation
2Benign Mutations, Animal Model

1 - 1 of 1

	PosAscending	Mutation	Protein	Primary	Exon/Intron	#Patients	#Alleles
	2268	c.2268-45T>G	(intronic)	Benign	Intron 18

1 - 1 of 1

c.2268-45T>G, (intronic)

The sequence variant c.2268-45T>G (dbSNP rs12984441) is located in intron 18. It has a minor allele frequency of 0.42 and is considered a common, benign SNP.

Mutation Details

Mutation type

Benign

Localization

Intron 18

Number of Patients

References

Riise Stensland et al. 2012

Primary Mutation Type Distribution