Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTCGCAGGGATCCAACCCTGTCCG[C/T]GTCTCCTTCGTAAACCTCAACGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 140571 | ||||||||||||||||||||
Literature Links: |
HSP90AA1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
HSP90AA1 - heat shock protein 90 alpha family class A member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017963.2 | 219 | Intron | NP_001017963.2 | |||
NM_005348.3 | 219 | Intron | NP_005339.3 | |||
XM_011536718.2 | 219 | Intron | XP_011535020.1 |
WDR20 - WD repeat domain 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242414.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001229343.1 | |
NM_001242415.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001229344.1 | |
NM_001242416.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001229345.1 | |
NM_001242417.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001229346.1 | |
NM_001242418.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001229347.1 | |
NM_001320130.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_001307059.1 | |
NM_144574.3 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_653175.2 | |
NM_181291.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_851808.1 | |
NM_181308.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | NP_851825.1 | |
XM_006720308.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_006720371.1 | |
XM_006720309.1 | 219 | Intron | XP_006720372.1 | |||
XM_006720310.1 | 219 | Intron | XP_006720373.1 | |||
XM_006720311.1 | 219 | Intron | XP_006720374.1 | |||
XM_006720313.2 | 219 | UTR 5 | XP_006720376.1 | |||
XM_006720318.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_006720381.1 | |
XM_006720320.3 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_006720383.1 | |
XM_011537335.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535637.1 | |
XM_011537336.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535638.1 | |
XM_011537337.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535639.1 | |
XM_011537338.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535640.1 | |
XM_011537339.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535641.1 | |
XM_011537340.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535642.1 | |
XM_011537341.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535643.1 | |
XM_011537343.1 | 219 | UTR 5 | XP_011535645.1 | |||
XM_011537344.2 | 219 | UTR 5 | XP_011535646.1 | |||
XM_011537345.1 | 219 | UTR 5 | XP_011535647.1 | |||
XM_011537346.1 | 219 | Intron | XP_011535648.1 | |||
XM_011537347.1 | 219 | Intron | XP_011535649.1 | |||
XM_011537352.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535654.1 | |
XM_011537353.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535655.1 | |
XM_011537355.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535657.1 | |
XM_011537356.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535658.1 | |
XM_011537358.2 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_011535660.1 | |
XM_017021766.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877255.1 | |
XM_017021767.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877256.1 | |
XM_017021768.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877257.1 | |
XM_017021770.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877259.1 | |
XM_017021771.1 | 219 | UTR 5 | XP_016877260.1 | |||
XM_017021772.1 | 219 | Intron | XP_016877261.1 | |||
XM_017021773.1 | 219 | Intron | XP_016877262.1 | |||
XM_017021774.1 | 219 | Intron | XP_016877263.1 | |||
XM_017021775.1 | 219 | Intron | XP_016877264.1 | |||
XM_017021776.1 | 219 | Intron | XP_016877265.1 | |||
XM_017021777.1 | 219 | Intron | XP_016877266.1 | |||
XM_017021778.1 | 219 | Intron | XP_016877267.1 | |||
XM_017021779.1 | 219 | Intron | XP_016877268.1 | |||
XM_017021780.1 | 219 | Intron | XP_016877269.1 | |||
XM_017021781.1 | 219 | UTR 5 | XP_016877270.1 | |||
XM_017021782.1 | 219 | Intron | XP_016877271.1 | |||
XM_017021783.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877272.1 | |
XM_017021784.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877273.1 | |
XM_017021785.1 | 219 | Silent Mutation | CGC,CGT | R,R 49 | XP_016877274.1 |