Product Details
- SNP ID
-
rs114485562
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:5316020 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAGGGGGATCCTGCCCGTGTCTCC[A/G]TCGTCAAACTCCACGGTGATCAAGT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TNRC18
PubMed Links
Gene Details
- Gene
- TNRC18
- Gene Name
- trinucleotide repeat containing 18
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001080495.2 |
9677 |
Silent Mutation |
GAC,GAT |
D2266D |
NP_001073964.2 |
| XM_017012728.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2277D |
XP_016868217.1 |
| XM_017012729.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2277D |
XP_016868218.1 |
| XM_017012730.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2276D |
XP_016868219.1 |
| XM_017012731.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2234D |
XP_016868220.1 |
| XM_017012732.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2233D |
XP_016868221.1 |
| XM_017012733.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2229D |
XP_016868222.1 |
| XM_017012734.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2227D |
XP_016868223.1 |
| XM_017012735.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2203D |
XP_016868224.1 |
| XM_017012736.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2203D |
XP_016868225.1 |
| XM_017012737.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2203D |
XP_016868226.1 |
| XM_017012738.1 |
9677 |
Silent Mutation |
GAC,GAT |
D2203D |
XP_016868227.1 |
| XM_017012739.1 |
9677 |
Intron |
|
|
XP_016868228.1 |
| XM_017012740.1 |
9677 |
Intron |
|
|
XP_016868229.1 |
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