Product Details

SNP ID: rs140875990
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:38213196 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAAGGTGGTGGCAAGCAAATGCTCG[C/T]GGGCAGGGTCAGGCAGCTTGTGGGA
Phenotype
Polymorphism: C/T, 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	3721	Missense Mutation			NP_001025035.1