Product Details
- SNP ID
-
rs113141592
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:67326913 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGGAAGGCATTCGCCGCCTGGGGGC[G/T]CTGACGCTGGAGCAGCCGGGTAGGG
- Phenotype
-
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
KCTD19
PubMed Links
Gene Details
- Gene
- KCTD19
- Gene Name
- potassium channel tetramerization domain containing 19
- Gene
- LRRC36
- Gene Name
- leucine rich repeat containing 36
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001161575.1 |
70 |
Intron |
|
|
NP_001155047.1 |
| NM_018296.5 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
NP_060766.5 |
| XM_005256025.2 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_005256082.1 |
| XM_005256026.2 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_005256083.1 |
| XM_005256027.2 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_005256084.1 |
| XM_005256028.1 |
70 |
UTR 5 |
|
|
XP_005256085.1 |
| XM_011523200.1 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_011521502.1 |
| XM_011523201.1 |
70 |
Intron |
|
|
XP_011521503.1 |
| XM_011523202.2 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_011521504.1 |
| XM_011523203.1 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_011521505.1 |
| XM_011523204.1 |
70 |
Intron |
|
|
XP_011521506.1 |
| XM_011523205.1 |
70 |
Intron |
|
|
XP_011521507.1 |
| XM_011523206.2 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_011521508.1 |
| XM_017023400.1 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_016878889.1 |
| XM_017023401.1 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_016878890.1 |
| XM_017023402.1 |
70 |
Silent Mutation |
GCG,GCT |
A17A |
XP_016878891.1 |
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