Product Details

SNP ID
rs41310426
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:33147226 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCGGCTGAACGTTCTTGCCATTG[A/G]CGTGGCTCTGGCCAGGGCTGAAGTA
Phenotype
MIM: 608353 MIM: 616755
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
AZIN2 PubMed Links

Gene Details

Gene
AZIN2
Gene Name
antizyme inhibitor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001293562.1 2017 Intron NP_001280491.1
NM_001301823.1 2017 Intron NP_001288752.1
NM_001301824.1 2017 Intron NP_001288753.1
NM_001301825.1 2017 Intron NP_001288754.1
NM_001301826.1 2017 Intron NP_001288755.1
NM_052998.3 2017 Intron NP_443724.1
XM_005270404.2 2017 Intron XP_005270461.1
XM_005270406.1 2017 Intron XP_005270463.1
XM_005270407.1 2017 Intron XP_005270464.1
XM_006710312.1 2017 Intron XP_006710375.1
XM_011540557.1 2017 Intron XP_011538859.1
XM_011540563.1 2017 Intron XP_011538865.1
XM_011540566.1 2017 Intron XP_011538868.1
XM_017000167.1 2017 Intron XP_016855656.1
XM_017000168.1 2017 Intron XP_016855657.1
XM_017000169.1 2017 Intron XP_016855658.1
XM_017000170.1 2017 Intron XP_016855659.1
XM_017000171.1 2017 Intron XP_016855660.1
XM_017000172.1 2017 Intron XP_016855661.1
XM_017000173.1 2017 Intron XP_016855662.1
XM_017000174.1 2017 Intron XP_016855663.1
XM_017000175.1 2017 Intron XP_016855664.1
XM_017000176.1 2017 Intron XP_016855665.1
XM_017000177.1 2017 Intron XP_016855666.1
XM_017000178.1 2017 Intron XP_016855667.1
Gene
TRIM62
Gene Name
tripartite motif containing 62
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018207.2 2017 Missense Mutation GCC,GTC A460V NP_060677.2
XM_011541705.2 2017 Missense Mutation GCC,GTC A339V XP_011540007.1
XM_017001629.1 2017 Missense Mutation GCC,GTC A540V XP_016857118.1
XM_017001630.1 2017 Missense Mutation GCC,GTC A529V XP_016857119.1
XM_017001631.1 2017 Intron XP_016857120.1

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