Product Details

SNP ID: rs146665662
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:38213296 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGCCTGCCTGGAAAGTTCTGTTCT[A/G]TTCCCCTCTGGGGGGCCCAGGAGGC
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KIAA1755 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029864.1	3621	Nonsense Mutation	CAG,TAG	Q1117*	NP_001025035.1