Product Details

SNP ID: rs190608612
Assay Type: Functionally tested
NCBI dbSNP Submissions: 11
Location: Chr.1:180916454 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTGGTCATCCCCCAAGAAACCCCA[A/G]TGCAGACGAGGCAAGGCAGGGAGAG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KIAA1614 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020950.1	418	Silent Mutation	CAA,CAG	Q117Q	NP_066001.1