Product Details

SNP ID: rs144628188
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:38213197 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGGTGGTGGCAAGCAAATGCTCGC[A/G]GGCAGGGTCAGGCAGCTTGTGGGAG
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	3720	Missense Mutation	CGC,TGC	R1150C	NP_001025035.1