Product Details
- SNP ID
-
rs138281148
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:102139983 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGATTAAGACCCAATTCACCACCCG[C/G]GAAGGTCTGTACAAGCTGCTGCCGC
- Phenotype
-
MIM: 140571
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
HSP90AA1
PubMed Links
Gene Details
- Gene
- HSP90AA1
- Gene Name
- heat shock protein 90 alpha family class A member 1
- Gene
- WDR20
- Gene Name
- WD repeat domain 20
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001242414.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001229343.1 |
NM_001242415.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001229344.1 |
NM_001242416.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001229345.1 |
NM_001242417.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001229346.1 |
NM_001242418.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001229347.1 |
NM_001320130.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_001307059.1 |
NM_144574.3 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_653175.2 |
NM_181291.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_851808.1 |
NM_181308.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
NP_851825.1 |
XM_006720308.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_006720371.1 |
XM_006720309.1 |
100 |
UTR 5 |
|
|
XP_006720372.1 |
XM_006720310.1 |
100 |
Intron |
|
|
XP_006720373.1 |
XM_006720311.1 |
100 |
UTR 5 |
|
|
XP_006720374.1 |
XM_006720313.2 |
100 |
UTR 5 |
|
|
XP_006720376.1 |
XM_006720318.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_006720381.1 |
XM_006720320.3 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_006720383.1 |
XM_011537335.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535637.1 |
XM_011537336.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535638.1 |
XM_011537337.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535639.1 |
XM_011537338.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535640.1 |
XM_011537339.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535641.1 |
XM_011537340.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535642.1 |
XM_011537341.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535643.1 |
XM_011537343.1 |
100 |
UTR 5 |
|
|
XP_011535645.1 |
XM_011537344.2 |
100 |
UTR 5 |
|
|
XP_011535646.1 |
XM_011537345.1 |
100 |
UTR 5 |
|
|
XP_011535647.1 |
XM_011537346.1 |
100 |
Intron |
|
|
XP_011535648.1 |
XM_011537347.1 |
100 |
Intron |
|
|
XP_011535649.1 |
XM_011537352.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535654.1 |
XM_011537353.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535655.1 |
XM_011537355.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535657.1 |
XM_011537356.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535658.1 |
XM_011537358.2 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_011535660.1 |
XM_017021766.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877255.1 |
XM_017021767.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877256.1 |
XM_017021768.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877257.1 |
XM_017021770.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877259.1 |
XM_017021771.1 |
100 |
UTR 5 |
|
|
XP_016877260.1 |
XM_017021772.1 |
100 |
UTR 5 |
|
|
XP_016877261.1 |
XM_017021773.1 |
100 |
UTR 5 |
|
|
XP_016877262.1 |
XM_017021774.1 |
100 |
UTR 5 |
|
|
XP_016877263.1 |
XM_017021775.1 |
100 |
UTR 5 |
|
|
XP_016877264.1 |
XM_017021776.1 |
100 |
UTR 5 |
|
|
XP_016877265.1 |
XM_017021777.1 |
100 |
Intron |
|
|
XP_016877266.1 |
XM_017021778.1 |
100 |
UTR 5 |
|
|
XP_016877267.1 |
XM_017021779.1 |
100 |
UTR 5 |
|
|
XP_016877268.1 |
XM_017021780.1 |
100 |
Intron |
|
|
XP_016877269.1 |
XM_017021781.1 |
100 |
UTR 5 |
|
|
XP_016877270.1 |
XM_017021782.1 |
100 |
UTR 5 |
|
|
XP_016877271.1 |
XM_017021783.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877272.1 |
XM_017021784.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877273.1 |
XM_017021785.1 |
100 |
Silent Mutation |
CGC,CGG |
R20R |
XP_016877274.1 |
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