Product Details
- SNP ID
-
rs142926499
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:40233919 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TAGGAGAACTGGGGGAAGTGGGTCC[A/G]CTGGTCCAGCTCCAGTAAGCCCAGG
- Phenotype
-
MIM: 164731
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
AKT2
PubMed Links
Gene Details
- Gene
- AKT2
- Gene Name
- AKT serine/threonine kinase 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001243027.2 |
1821 |
Missense Mutation |
CGG,TGG |
R405W |
NP_001229956.1 |
NM_001243028.2 |
1821 |
Missense Mutation |
CGG,TGG |
R405W |
NP_001229957.1 |
NM_001626.5 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
NP_001617.1 |
XM_011526614.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524916.1 |
XM_011526615.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524917.1 |
XM_011526616.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524918.1 |
XM_011526618.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524920.1 |
XM_011526619.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524921.1 |
XM_011526620.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_011524922.1 |
XM_011526622.2 |
1821 |
Intron |
|
|
XP_011524924.1 |
XM_017026470.1 |
1821 |
Missense Mutation |
CGG,TGG |
R467W |
XP_016881959.1 |
XM_017026471.1 |
1821 |
Missense Mutation |
CGG,TGG |
R424W |
XP_016881960.1 |
- Gene
- CNTD2
- Gene Name
- cyclin N-terminal domain containing 2
There are no transcripts associated with this gene.
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