Product Details
- SNP ID
-
rs142601219
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:30185984 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTAGATGAGTTCCTGTGACTCTGC[A/G]TTGGTGAAAGTCACGGTGCCCCCTT
- Phenotype
-
MIM: 600830
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TRIM26
PubMed Links
Gene Details
- Gene
- TRIM26
- Gene Name
- tripartite motif containing 26
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001242783.1 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
NP_001229712.1 |
| NM_003449.4 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
NP_003440.1 |
| XM_005249374.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_005249431.1 |
| XM_005249375.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_005249432.1 |
| XM_005249376.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_005249433.1 |
| XM_005249377.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_005249434.1 |
| XM_005249378.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_005249435.1 |
| XM_006715180.2 |
1642 |
Silent Mutation |
AAC,AAT |
N504N |
XP_006715243.1 |
| XM_011514859.1 |
1642 |
Silent Mutation |
AAC,AAT |
N427N |
XP_011513161.1 |
| XM_017011263.1 |
1642 |
Silent Mutation |
AAC,AAT |
N427N |
XP_016866752.1 |
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