Product Details

SNP ID: rs201795862
Assay Type: Functionally tested
NCBI dbSNP Submissions: 4
Location: Chr.1:92168939 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGGTTCAGTCTTTCTATGCTGTTC[A/G]TCACACAGAAAGCTGGAAGCTGATG
Phenotype
Polymorphism: A/G, 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	19	UTR 5			XP_016856289.1