Product Details

SNP ID: rs61729581
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:32528528 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCTACCACCACTCACACCAGGGCC[A/T]CCTGGAGAGCCAGTCTTTTTACTCA
Phenotype: MIM: 615890
Polymorphism: A/T, 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	1484	Silent Mutation	GGA,GGT	G460G	NP_057225.2