Product Details

SNP ID: rs499588
Assay Type: Functionally tested
NCBI dbSNP Submissions: 9
Location: Chr.1:92176567 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCAAAACTTCATACATTAAAAAAGC[C/T]TTCCTTTTATTTATTTATTTACTTT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: KIAA1107 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017000800.1		Intron			XP_016856289.1