Product Details

SNP ID
rs55784699
Assay Type
Functionally tested
NCBI dbSNP Submissions
19
Location
Chr.1:114397764 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATCCTCTTCCTGCTCAAACTCTG[G/T]CAAAGGTGCGAAGGTCCTGTCTGAG
Phenotype
MIM: 605769
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TRIM33 PubMed Links

Gene Details

Gene
TRIM33
Gene Name
tripartite motif containing 33
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015906.3 2627 Missense Mutation NP_056990.3
NM_033020.2 2627 Missense Mutation NP_148980.2
XM_005270936.3 2627 Missense Mutation XP_005270993.1
XM_005270937.3 2627 Missense Mutation XP_005270994.1
XM_011541568.2 2627 Missense Mutation XP_011539870.1
XM_017001452.1 2627 Missense Mutation XP_016856941.1
XM_017001453.1 2627 Missense Mutation XP_016856942.1
XM_017001454.1 2627 Intron XP_016856943.1

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