Product Details

SNP ID
rs201217931
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:111542250 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGTGTAAGGTGTTCAGAAGACAA[C/T]GGAGAAAAAATGGAAATACTGTGCT
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_001318889.1 172 Missense Mutation ACG,ATG T1M NP_001305818.1
NM_005816.4 172 Missense Mutation ACG,ATG T1M NP_005807.1
NM_198196.2 172 Missense Mutation ACG,ATG T1M NP_937839.1
XM_005247063.3 172 Missense Mutation ACG,ATG T1M XP_005247120.1
XM_006713469.3 172 Missense Mutation ACG,ATG T1M XP_006713532.1
XM_006713470.3 172 Missense Mutation ACG,ATG T1M XP_006713533.1
XM_017005521.1 172 Missense Mutation ACG,ATG T1M XP_016861010.1
XM_017005522.1 172 Missense Mutation ACG,ATG T1M XP_016861011.1

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