Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603709 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAM22 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ADAM22 - ADAM metallopeptidase domain 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324417.1 | 457 | Missense Mutation | CCG,CGG | P,R 80 | NP_001311346.1 | |
NM_001324418.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_001311347.1 | |
NM_001324419.1 | 457 | Missense Mutation | CCG,CGG | P,R 80 | NP_001311348.1 | |
NM_001324420.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_001311349.1 | |
NM_001324421.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_001311350.1 | |
NM_004194.4 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_004185.1 | |
NM_016351.5 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_057435.2 | |
NM_021721.4 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_068367.1 | |
NM_021722.5 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_068368.2 | |
NM_021723.4 | 457 | Missense Mutation | CCG,CGG | P,R 81 | NP_068369.1 | |
XM_005250445.3 | 457 | Missense Mutation | CCG,CGG | P,R 133 | XP_005250502.1 | |
XM_006716028.3 | 457 | Missense Mutation | CCG,CGG | P,R 133 | XP_006716091.1 | |
XM_006716029.3 | 457 | Missense Mutation | CCG,CGG | P,R 133 | XP_006716092.1 | |
XM_011516318.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_011514620.1 | |
XM_011516319.2 | 457 | Missense Mutation | CCG,CGG | P,R 80 | XP_011514621.1 | |
XM_011516320.2 | 457 | Missense Mutation | CCG,CGG | P,R 133 | XP_011514622.1 | |
XM_011516321.2 | 457 | Missense Mutation | CCG,CGG | P,R 133 | XP_011514623.1 | |
XM_011516322.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_011514624.1 | |
XM_011516323.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_011514625.1 | |
XM_011516324.1 | 457 | Intron | XP_011514626.1 | |||
XM_017012329.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867818.1 | |
XM_017012330.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867819.1 | |
XM_017012331.1 | 457 | Missense Mutation | CCG,CGG | P,R 80 | XP_016867820.1 | |
XM_017012332.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867821.1 | |
XM_017012333.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867822.1 | |
XM_017012334.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867823.1 | |
XM_017012335.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867824.1 | |
XM_017012336.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867825.1 | |
XM_017012337.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867826.1 | |
XM_017012338.1 | 457 | Missense Mutation | CCG,CGG | P,R 80 | XP_016867827.1 | |
XM_017012339.1 | 457 | Missense Mutation | CCG,CGG | P,R 81 | XP_016867828.1 | |
XM_017012340.1 | 457 | Intron | XP_016867829.1 | |||
XM_017012341.1 | 457 | UTR 5 | XP_016867830.1 |
Set Membership: |
HapMap |