Product Details

SNP ID
rs142008016
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:16317222 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTGTGCATTTCTTCTCTGGAGAAT[C/T]GCCACTGAAACTAGAAATCAGAAAG
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
OXNAD1 PubMed Links

Gene Details

Gene
OXNAD1
Gene Name
oxidoreductase NAD binding domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138381.3 1650 Intron NP_612390.1
XM_005265559.3 1650 Intron XP_005265616.1
XM_006713405.1 1650 Intron XP_006713468.1
XM_006713406.2 1650 Intron XP_006713469.1
XM_011534230.2 1650 Intron XP_011532532.1
XM_011534232.2 1650 Intron XP_011532534.1
XM_011534233.2 1650 Intron XP_011532535.1
XM_011534234.2 1650 Intron XP_011532536.1
XM_011534235.2 1650 Intron XP_011532537.1
XM_017007485.1 1650 Intron XP_016862974.1
XM_017007486.1 1650 Intron XP_016862975.1
XM_017007487.1 1650 Intron XP_016862976.1
XM_017007488.1 1650 Intron XP_016862977.1
XM_017007489.1 1650 Intron XP_016862978.1
XM_017007490.1 1650 Intron XP_016862979.1
XM_017007491.1 1650 Intron XP_016862980.1
XM_017007492.1 1650 Intron XP_016862981.1
XM_017007493.1 1650 Intron XP_016862982.1
XM_017007494.1 1650 Intron XP_016862983.1
XM_017007495.1 1650 Intron XP_016862984.1
XM_017007496.1 1650 Intron XP_016862985.1
Gene
RFTN1
Gene Name
raftlin, lipid raft linker 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015150.1 1650 Missense Mutation CAA,CGA Q448R NP_055965.1
XM_005264985.1 1650 Missense Mutation CAA,CGA Q448R XP_005265042.1
XM_005264986.2 1650 Missense Mutation CAA,CGA Q448R XP_005265043.1
XM_006713069.1 1650 Missense Mutation CAA,CGA Q448R XP_006713132.1
XM_011533529.1 1650 Missense Mutation CAA,CGA Q483R XP_011531831.1
XM_011533530.1 1650 Missense Mutation CAA,CGA Q448R XP_011531832.1
XM_011533531.1 1650 Silent Mutation GCA,GCG A444A XP_011531833.1
XM_017006005.1 1650 Intron XP_016861494.1
XM_017006006.1 1650 Intron XP_016861495.1
XM_017006007.1 1650 Silent Mutation GCA,GCG A409A XP_016861496.1

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