Product Details
- SNP ID
-
rs61999299
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
1
- Location
-
Chr.1:51288878 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGTTTGATGGCCTCTTCGTTTCTG[G/T]CTTGCTCCATAAGCAGCAGGGCCAG
- Phenotype
-
- Polymorphism
- G/T, Transversion 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 |
1778 |
Missense Mutation |
GAC,GCC |
D525A |
NP_001073963.1 |
NM_001144832.2 |
1778 |
Missense Mutation |
GAC,GCC |
D528A |
NP_001138304.1 |
NM_001297662.1 |
1778 |
Intron |
|
|
NP_001284591.1 |
NM_001297663.1 |
1778 |
Missense Mutation |
GAC,GCC |
D524A |
NP_001284592.1 |
NM_001297664.1 |
1778 |
Missense Mutation |
GAC,GCC |
D497A |
NP_001284593.1 |
NM_001297665.1 |
1778 |
Missense Mutation |
GAC,GCC |
D560A |
NP_001284594.1 |
NM_001297666.1 |
1778 |
Missense Mutation |
GAC,GCC |
D168A |
NP_001284595.1 |
NM_001297667.1 |
1778 |
Missense Mutation |
GAC,GCC |
D101A |
NP_001284596.1 |
XM_005270644.2 |
1778 |
Missense Mutation |
GAC,GCC |
D521A |
XP_005270701.1 |
XM_006710471.2 |
1778 |
Missense Mutation |
GAC,GCC |
D556A |
XP_006710534.1 |
XM_011541048.2 |
1778 |
Missense Mutation |
GAC,GCC |
D563A |
XP_011539350.1 |
XM_011541049.2 |
1778 |
Missense Mutation |
GAC,GCC |
D561A |
XP_011539351.1 |
XM_011541050.2 |
1778 |
Missense Mutation |
GAC,GCC |
D559A |
XP_011539352.1 |
XM_011541051.2 |
1778 |
Missense Mutation |
GAC,GCC |
D532A |
XP_011539353.1 |
XM_011541052.2 |
1778 |
Missense Mutation |
GAC,GCC |
D532A |
XP_011539354.1 |
XM_011541053.2 |
1778 |
Missense Mutation |
GAC,GCC |
D532A |
XP_011539355.1 |
XM_011541054.2 |
1778 |
Missense Mutation |
GAC,GCC |
D497A |
XP_011539356.1 |
XM_017000715.1 |
1778 |
Missense Mutation |
GAC,GCC |
D497A |
XP_016856204.1 |
View Full Product Details