Product Details

SNP ID
rs530702
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:120113123 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCTGCATAAATTTCCCTTACAGAA[A/G]GGGTGCAGAGAGGGTAAAGAACTGC
Phenotype
MIM: 610658
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TRIM29 PubMed Links

Gene Details

Gene
TRIM29
Gene Name
tripartite motif containing 29
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012101.3 Intron NP_036233.2
XM_005271490.1 Intron XP_005271547.1
XM_011542729.1 Intron XP_011541031.1
XM_011542732.1 Intron XP_011541034.1
XM_011542733.1 Intron XP_011541035.1
XM_017017453.1 Intron XP_016872942.1
XM_017017454.1 Intron XP_016872943.1

View Full Product Details