Product Details

SNP ID: rs116363983
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:32526079 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCAAAGCCATATATATATATATAT[A/G]TGTATAGACAAATCCAAAGATTGTT
Phenotype: MIM: 615890
Polymorphism: A/G, Transition 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	2396	UTR 3			NP_057225.2