Product Details
- SNP ID
-
rs138760260
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
6
- Location
-
Chr.1:247300631 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GACGCAGTACCGGCACTGGAAGGGC[C/T]GGGCTTTGTCCTTCAGGTGAAAGTG
- Phenotype
-
MIM: 613911
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF496
PubMed Links
Gene Details
- Gene
- ZNF496
- Gene Name
- zinc finger protein 496
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| XM_005273328.3 |
3608 |
Missense Mutation |
CAG,CGG |
Q587R |
XP_005273385.1 |
| XM_005273330.3 |
3608 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_005273387.1 |
| XM_006711838.2 |
3608 |
Intron |
|
|
XP_006711901.1 |
| XM_011544310.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q618R |
XP_011542612.1 |
| XM_011544312.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q582R |
XP_011542614.1 |
| XM_011544314.2 |
3608 |
Intron |
|
|
XP_011542616.1 |
| XM_011544315.2 |
3608 |
Intron |
|
|
XP_011542617.1 |
| XM_011544316.1 |
3608 |
Intron |
|
|
XP_011542618.1 |
| XM_017002586.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q649R |
XP_016858075.1 |
| XM_017002587.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q629R |
XP_016858076.1 |
| XM_017002588.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q618R |
XP_016858077.1 |
| XM_017002589.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q613R |
XP_016858078.1 |
| XM_017002590.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q582R |
XP_016858079.1 |
| XM_017002591.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q531R |
XP_016858080.1 |
| XM_017002592.1 |
3608 |
Intron |
|
|
XP_016858081.1 |
| XM_017002593.1 |
3608 |
Intron |
|
|
XP_016858082.1 |
| XM_017002594.1 |
3608 |
Missense Mutation |
CAG,CGG |
Q354R |
XP_016858083.1 |
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