Product Details

SNP ID: rs12756225
Assay Type: Functionally tested
NCBI dbSNP Submissions: 1
Location: Chr.1:180913259 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTCCGAGGGATGGAGGGGACAGAG[G/T]CGGCGGCGGCCAAACCCGCGGGCGG
Phenotype
Polymorphism: G/T, Transversion 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	83	Missense Mutation	GCG,TCG	A6S	NP_066001.1