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Search Thermo Fisher Scientific
AAGAGGAAGGAAAACCGCTTCGTGG[A/T]GCGCCAGAGCATCGTGCCACTGCGC
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 | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
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 | 352 | Missense Mutation | GAG,GTG | E,V 45 | NP_001311346.1 | |
NM_001324418.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_001311347.1 | |
NM_001324419.1 | 352 | Missense Mutation | GAG,GTG | E,V 45 | NP_001311348.1 | |
NM_001324420.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_001311349.1 | |
NM_001324421.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_001311350.1 | |
NM_004194.4 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_004185.1 | |
NM_016351.5 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_057435.2 | |
NM_021721.4 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_068367.1 | |
NM_021722.5 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_068368.2 | |
NM_021723.4 | 352 | Missense Mutation | GAG,GTG | E,V 46 | NP_068369.1 | |
XM_005250445.3 | 352 | Missense Mutation | GAG,GTG | E,V 98 | XP_005250502.1 | |
XM_006716028.3 | 352 | Missense Mutation | GAG,GTG | E,V 98 | XP_006716091.1 | |
XM_006716029.3 | 352 | Missense Mutation | GAG,GTG | E,V 98 | XP_006716092.1 | |
XM_011516318.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_011514620.1 | |
XM_011516319.2 | 352 | Missense Mutation | GAG,GTG | E,V 45 | XP_011514621.1 | |
XM_011516320.2 | 352 | Missense Mutation | GAG,GTG | E,V 98 | XP_011514622.1 | |
XM_011516321.2 | 352 | Missense Mutation | GAG,GTG | E,V 98 | XP_011514623.1 | |
XM_011516322.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_011514624.1 | |
XM_011516323.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_011514625.1 | |
XM_011516324.1 | 352 | Intron | XP_011514626.1 | |||
XM_017012329.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867818.1 | |
XM_017012330.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867819.1 | |
XM_017012331.1 | 352 | Missense Mutation | GAG,GTG | E,V 45 | XP_016867820.1 | |
XM_017012332.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867821.1 | |
XM_017012333.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867822.1 | |
XM_017012334.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867823.1 | |
XM_017012335.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867824.1 | |
XM_017012336.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867825.1 | |
XM_017012337.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867826.1 | |
XM_017012338.1 | 352 | Missense Mutation | GAG,GTG | E,V 45 | XP_016867827.1 | |
XM_017012339.1 | 352 | Missense Mutation | GAG,GTG | E,V 46 | XP_016867828.1 | |
XM_017012340.1 | 352 | Intron | XP_016867829.1 | |||
XM_017012341.1 | 352 | UTR 5 | XP_016867830.1 |