Product Details

SNP ID: rs138056597
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:32528533 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCACCACTCACACCAGGGCCTCCTG[A/G]AGAGCCAGTCTTTTTACTCAACAAA
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	1479	Missense Mutation	CCA,TCA	P459S	NP_057225.2