Product Details

SNP ID
rs139743881
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:111545337 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCAGTCAGTGGAAGGTACGAGT[C/G]TATGCTTGTTCTGTATCCAGAGGGC
Phenotype
MIM: 606037
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CD96 PubMed Links

Gene Details

Gene
CD96
Gene Name
CD96 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318889.1 523 Missense Mutation TCT,TGT S118C NP_001305818.1
NM_005816.4 523 Missense Mutation TCT,TGT S118C NP_005807.1
NM_198196.2 523 Missense Mutation TCT,TGT S118C NP_937839.1
XM_005247063.3 523 Missense Mutation TCT,TGT S118C XP_005247120.1
XM_006713469.3 523 Missense Mutation TCT,TGT S118C XP_006713532.1
XM_006713470.3 523 Missense Mutation TCT,TGT S118C XP_006713533.1
XM_017005521.1 523 Missense Mutation TCT,TGT S118C XP_016861010.1
XM_017005522.1 523 Missense Mutation TCT,TGT S118C XP_016861011.1

View Full Product Details