Product Details

SNP ID
rs140137237
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:111545143 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAAACACAGACAGTAGGCTTCTT[C/T]GTGCAGATGCAATGGTCCAAGGTCA
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_001318889.1 329 Silent Mutation TTC,TTT F53F NP_001305818.1
NM_005816.4 329 Silent Mutation TTC,TTT F53F NP_005807.1
NM_198196.2 329 Silent Mutation TTC,TTT F53F NP_937839.1
XM_005247063.3 329 Silent Mutation TTC,TTT F53F XP_005247120.1
XM_006713469.3 329 Silent Mutation TTC,TTT F53F XP_006713532.1
XM_006713470.3 329 Silent Mutation TTC,TTT F53F XP_006713533.1
XM_017005521.1 329 Silent Mutation TTC,TTT F53F XP_016861010.1
XM_017005522.1 329 Silent Mutation TTC,TTT F53F XP_016861011.1

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