Product Details

SNP ID
rs13114864
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:153166153 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGTTCTTATTTCACGGATGCAATA[G/T]CTTTTTTTTGCTCTGAAGATACTAA
Phenotype
MIM: 614141
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
TRIM2 PubMed Links

Gene Details

Gene
TRIM2
Gene Name
tripartite motif containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130067.1 Intron NP_001123539.1
NM_001302692.1 Intron NP_001289621.1
NM_001302693.1 Intron NP_001289622.1
NM_001302694.1 Intron NP_001289623.1
NM_015271.4 Intron NP_056086.2
XM_006714157.1 Intron XP_006714220.1
XM_006714158.1 Intron XP_006714221.1
XM_006714159.3 Intron XP_006714222.1
XM_006714160.1 Intron XP_006714223.1
XM_006714161.1 Intron XP_006714224.1
XM_006714162.1 Intron XP_006714225.1
XM_006714165.3 Intron XP_006714228.1
XM_011531794.1 Intron XP_011530096.1
XM_011531795.1 Intron XP_011530097.1
XM_011531796.2 Intron XP_011530098.1
XM_011531798.2 Intron XP_011530100.1
XM_017007943.1 Intron XP_016863432.1
XM_017007944.1 Intron XP_016863433.1
XM_017007945.1 Intron XP_016863434.1
XM_017007946.1 Intron XP_016863435.1
XM_017007947.1 Intron XP_016863436.1
XM_017007948.1 Intron XP_016863437.1
XM_017007949.1 Intron XP_016863438.1
XM_017007950.1 Intron XP_016863439.1
XM_017007951.1 Intron XP_016863440.1
XM_017007952.1 Intron XP_016863441.1
XM_017007953.1 Intron XP_016863442.1
XM_017007954.1 Intron XP_016863443.1
XM_017007955.1 Intron XP_016863444.1

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