Product Details

SNP ID: rs111395778
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:32526848 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGATGTAGGTGTTGTGGGAGAAACT[C/G]TAACTGGTTTTCGTGTAATTCTGTC
Phenotype: MIM: 615890
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: DYNC1LI1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016141.3	1627	Missense Mutation	ACA,AGA	T508R	NP_057225.2