Product Details
- SNP ID
-
rs4726019
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:151381633 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGCAGCCCACCTTGTTGCTGAAGAG[A/C]CGCGAGAGGCTGCGCATGGGCGGAG
- Phenotype
-
MIM: 607981
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NUB1
PubMed Links
Gene Details
- Gene
- NUB1
- Gene Name
- negative regulator of ubiquitin like proteins 1
There are no transcripts associated with this gene.
- Gene
- WDR86
- Gene Name
- WD repeat domain 86
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001284260.1 |
1526 |
Missense Mutation |
GCT,TCT |
A382S |
NP_001271189.1 |
NM_001284261.1 |
1526 |
Missense Mutation |
GGC,GTC |
G187V |
NP_001271190.1 |
NM_001284262.1 |
1526 |
Silent Mutation |
CGG,CGT |
R232R |
NP_001271191.1 |
NM_198285.2 |
1526 |
Silent Mutation |
CGG,CGT |
R360R |
NP_938026.2 |
XM_005249989.3 |
1526 |
Missense Mutation |
GGC,GTC |
G315V |
XP_005250046.1 |
XM_005249990.4 |
1526 |
Intron |
|
|
XP_005250047.1 |
XM_006715966.2 |
1526 |
Intron |
|
|
XP_006716029.1 |
XM_011516144.2 |
1526 |
Missense Mutation |
GCT,TCT |
A382S |
XP_011514446.1 |
XM_011516145.2 |
1526 |
Intron |
|
|
XP_011514447.1 |
XM_011516146.2 |
1526 |
Silent Mutation |
CGG,CGT |
R360R |
XP_011514448.1 |
XM_011516147.2 |
1526 |
Missense Mutation |
GGC,GTC |
G315V |
XP_011514449.1 |
XM_011516148.1 |
1526 |
Missense Mutation |
GCT,TCT |
A254S |
XP_011514450.1 |
XM_011516150.1 |
1526 |
Missense Mutation |
GCT,TCT |
A254S |
XP_011514452.1 |
XM_011516151.2 |
1526 |
Intron |
|
|
XP_011514453.1 |
XM_011516152.1 |
1526 |
Intron |
|
|
XP_011514454.1 |
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