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CCAGTAACAGTTCAATATGGGGGAC[A/G]TTCTGGCTCATGAATCTGAATTACT
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 | |||
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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
|
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 | 49 | Missense Mutation | ATT,GTT | I,V 4 | NP_001258395.1 | |
NM_001291656.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | NP_001278585.1 | |
NM_025139.5 | 49 | Missense Mutation | ATT,GTT | I,V 4 | NP_079415.3 | |
XM_011511905.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510207.1 | |
XM_011511906.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510208.1 | |
XM_011511907.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510209.1 | |
XM_011511908.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510210.1 | |
XM_011511909.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510211.1 | |
XM_011511910.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510212.1 | |
XM_011511911.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510213.1 | |
XM_011511912.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510214.1 | |
XM_011511913.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510215.1 | |
XM_011511914.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510216.1 | |
XM_011511915.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510217.1 | |
XM_011511916.2 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_011510218.1 | |
XM_011511919.2 | 49 | Intron | XP_011510221.1 | |||
XM_017005018.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860507.1 | |
XM_017005019.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860508.1 | |
XM_017005020.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860509.1 | |
XM_017005021.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860510.1 | |
XM_017005022.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860511.1 | |
XM_017005023.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860512.1 | |
XM_017005024.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860513.1 | |
XM_017005025.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860514.1 | |
XM_017005026.1 | 49 | Missense Mutation | ATT,GTT | I,V 4 | XP_016860515.1 |