Mutations

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ToggleEditMutation = 'c.1310-22T>C'
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Mutation
2Benign Mutations, Animal Model

1 - 1 of 1

	PosAscending	Mutation	Protein	Primary	Exon/Intron	#Patients	#Alleles
	1310	c.1310-22T>C	(intronic)	Benign	Intron 10

1 - 1 of 1

c.1310-22T>C, (intronic)

The sequence variant c.1310-22T>C (dbSNP rs73002392) is located in intron 10. It has a minor allele frequency of 0.41, and is considered a common, benign SNP.

Mutation Details

Mutation type

Benign

Localization

Intron 10

Number of Patients

References

Riise Stensland et al. 2012

Primary Mutation Type Distribution