Product Details

SNP ID
rs141152689
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:69957450 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGGCTGAGGAACAGACCACAGGG[A/G]CTGAGGGGGAAGTGCAAGAGTCTGA
Phenotype
MIM: 115460
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CSN2 PubMed Links

Gene Details

Gene
CSN2
Gene Name
casein beta
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001302770.1 515 Missense Mutation CCC,TCC P166S NP_001289699.1
NM_001891.3 515 Missense Mutation CCC,TCC P167S NP_001882.1
XM_017007760.1 515 Missense Mutation CCC,TCC P167S XP_016863249.1

View Full Product Details