Product Details

SNP ID
rs143899586
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:51290048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAATTCTCCTCGGCCTCCTGGACAC[A/G]GCCCAGGTATTTCAGACACAGGCCT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TTC39A PubMed Links

Gene Details

Gene
TTC39A
Gene Name
tetratricopeptide repeat domain 39A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080494.3 1657 Missense Mutation NP_001073963.1
NM_001144832.2 1657 Missense Mutation NP_001138304.1
NM_001297662.1 1657 Intron NP_001284591.1
NM_001297663.1 1657 Missense Mutation NP_001284592.1
NM_001297664.1 1657 Missense Mutation NP_001284593.1
NM_001297665.1 1657 Missense Mutation NP_001284594.1
NM_001297666.1 1657 Missense Mutation NP_001284595.1
NM_001297667.1 1657 Missense Mutation NP_001284596.1
XM_005270644.2 1657 Missense Mutation XP_005270701.1
XM_006710471.2 1657 Missense Mutation XP_006710534.1
XM_011541048.2 1657 Missense Mutation XP_011539350.1
XM_011541049.2 1657 Missense Mutation XP_011539351.1
XM_011541050.2 1657 Missense Mutation XP_011539352.1
XM_011541051.2 1657 Missense Mutation XP_011539353.1
XM_011541052.2 1657 Missense Mutation XP_011539354.1
XM_011541053.2 1657 Missense Mutation XP_011539355.1
XM_011541054.2 1657 Missense Mutation XP_011539356.1
XM_017000715.1 1657 Missense Mutation XP_016856204.1

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