Product Details

SNP ID
rs146387805
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:111545314 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTGCACTTAAGGAATATGTCTTG[C/T]TCAGTCAGTGGAAGGTACGAGTGTA
Phenotype
MIM: 606037
Polymorphism
C/T, Transition 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_001318889.1 500 Silent Mutation TGC,TGT C110C NP_001305818.1
NM_005816.4 500 Silent Mutation TGC,TGT C110C NP_005807.1
NM_198196.2 500 Silent Mutation TGC,TGT C110C NP_937839.1
XM_005247063.3 500 Silent Mutation TGC,TGT C110C XP_005247120.1
XM_006713469.3 500 Silent Mutation TGC,TGT C110C XP_006713532.1
XM_006713470.3 500 Silent Mutation TGC,TGT C110C XP_006713533.1
XM_017005521.1 500 Silent Mutation TGC,TGT C110C XP_016861010.1
XM_017005522.1 500 Silent Mutation TGC,TGT C110C XP_016861011.1

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