Product Details
- SNP ID
-
rs199586267
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:9413474 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTAGGGTTTTTCTCCAGTGTGGATC[C/T]GCATGTGAAGGTTAACACACGTGGG
- Phenotype
-
MIM: 604751
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF266
PubMed Links
Gene Details
- Gene
- ZNF266
- Gene Name
- zinc finger protein 266
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001271314.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
NP_001258243.1 |
NM_006631.3 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
NP_006622.2 |
XM_005259716.3 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_005259773.1 |
XM_006722620.2 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_006722683.1 |
XM_006722621.2 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_006722684.1 |
XM_006722622.2 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_006722685.1 |
XM_006722623.3 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_006722686.1 |
XM_006722627.2 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_006722690.1 |
XM_006722630.2 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_006722693.1 |
XM_011527644.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_011525946.1 |
XM_011527647.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_011525949.1 |
XM_011527648.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_011525950.1 |
XM_011527650.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_011525952.1 |
XM_017026154.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_016881643.1 |
XM_017026155.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q551R |
XP_016881644.1 |
XM_017026156.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881645.1 |
XM_017026157.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881646.1 |
XM_017026158.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881647.1 |
XM_017026159.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881648.1 |
XM_017026160.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881649.1 |
XM_017026161.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881650.1 |
XM_017026162.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881651.1 |
XM_017026163.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881652.1 |
XM_017026164.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881653.1 |
XM_017026165.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881654.1 |
XM_017026166.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881655.1 |
XM_017026167.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q484R |
XP_016881656.1 |
XM_017026168.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q254R |
XP_016881657.1 |
XM_017026169.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q254R |
XP_016881658.1 |
XM_017026170.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q254R |
XP_016881659.1 |
XM_017026171.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q254R |
XP_016881660.1 |
XM_017026172.1 |
2310 |
Missense Mutation |
CAG,CGG |
Q254R |
XP_016881661.1 |
XM_017026173.1 |
2310 |
UTR 3 |
|
|
XP_016881662.1 |
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