Product Details

SNP ID: rs143517124
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:32526908 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATGAACATCTAAGACAGGCTTCTGG[A/C]CTACATTGAAGAAAAAGAAAAAAAA
Phenotype: MIM: 615890
Polymorphism: A/C, 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	1567	Missense Mutation	GGC,GTC	G488V	NP_057225.2