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Search Thermo Fisher Scientific
GAAAACCATTGTGTAAAACAGTAGG[C/T]GGATCTTTCAGAGACTCCAAATCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ARMC9 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
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Caucasian
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ARMC9 - armadillo repeat containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271466.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | NP_001258395.1 | |
NM_001291656.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | NP_001278585.1 | |
NM_025139.5 | 180 | Silent Mutation | GGC,GGT | G,G 47 | NP_079415.3 | |
XM_011511905.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510207.1 | |
XM_011511906.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510208.1 | |
XM_011511907.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510209.1 | |
XM_011511908.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510210.1 | |
XM_011511909.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510211.1 | |
XM_011511910.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510212.1 | |
XM_011511911.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510213.1 | |
XM_011511912.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510214.1 | |
XM_011511913.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510215.1 | |
XM_011511914.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510216.1 | |
XM_011511915.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510217.1 | |
XM_011511916.2 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_011510218.1 | |
XM_011511919.2 | 180 | Intron | XP_011510221.1 | |||
XM_017005018.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860507.1 | |
XM_017005019.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860508.1 | |
XM_017005020.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860509.1 | |
XM_017005021.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860510.1 | |
XM_017005022.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860511.1 | |
XM_017005023.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860512.1 | |
XM_017005024.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860513.1 | |
XM_017005025.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860514.1 | |
XM_017005026.1 | 180 | Silent Mutation | GGC,GGT | G,G 47 | XP_016860515.1 |
Set Membership: |
Validated |