Product Details
- SNP ID
-
rs113956278
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:123726173 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCACATTCGTTGCATCGGCAGGGCC[C/T]CACTGAGGCGTGTCCTCTCAAGTGC
- Phenotype
-
MIM: 603430
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF202
PubMed Links
Gene Details
- Gene
- ZNF202
- Gene Name
- zinc finger protein 202
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001301779.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
NP_001288708.1 |
NM_001301780.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
NP_001288709.1 |
NM_001301819.1 |
2371 |
Missense Mutation |
AGG,GGG |
R367G |
NP_001288748.1 |
NM_003455.3 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
NP_003446.2 |
XM_005271659.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_005271716.1 |
XM_005271660.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_005271717.1 |
XM_005271661.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_005271718.1 |
XM_005271664.1 |
2371 |
Missense Mutation |
AGG,GGG |
R367G |
XP_005271721.1 |
XM_006718901.2 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_006718964.1 |
XM_011542972.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_011541274.1 |
XM_011542973.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_011541275.1 |
XM_011542975.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_011541277.1 |
XM_011542976.1 |
2371 |
Missense Mutation |
AGG,GGG |
R367G |
XP_011541278.1 |
XM_017018268.1 |
2371 |
Missense Mutation |
AGG,GGG |
R591G |
XP_016873757.1 |
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