Product Details

SNP ID: rs200317123
Assay Type: Functionally tested
NCBI dbSNP Submissions: 6
Location: Chr.1:180916562 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAACCTGCCTGATGGGCAGCTGGA[C/T]GGCAGCATCAATGAGGAGCAACCCG
Phenotype
Polymorphism: C/T, 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	526	Silent Mutation	GAC,GAT	D153D	NP_066001.1