Product Details

SNP ID: rs2142551
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:45286394 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCCCATTACAGAGCAGGGAAGCAAG[C/G]CTCAGAGAGGTGGAATAACCCCCCC
Phenotype: MIM: 611559
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: UPK3A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167574.1		Intron			NP_001161046.1
NM_006953.3		Intron			NP_008884.1