Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615929 MIM: 610428 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD17 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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ANKRD17 - ankyrin repeat domain 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286771.2 | 7108 | Silent Mutation | ACA,ACG | T,T 2464 | NP_001273700.1 | |
NM_015574.1 | 7108 | Silent Mutation | ACA,ACG | T,T 2576 | NP_056389.1 | |
NM_032217.4 | 7108 | Silent Mutation | ACA,ACG | T,T 2577 | NP_115593.3 | |
NM_198889.2 | 7108 | Silent Mutation | ACA,ACG | T,T 2326 | NP_942592.1 | |
XM_005265671.3 | 7108 | Silent Mutation | ACA,ACG | T,T 2325 | XP_005265728.1 | |
XM_005265672.3 | 7108 | Intron | XP_005265729.1 | |||
XM_005265673.3 | 7108 | Intron | XP_005265730.1 | |||
XM_017008011.1 | 7108 | Silent Mutation | ACA,ACG | T,T 2463 | XP_016863500.1 | |
XM_017008012.1 | 7108 | Silent Mutation | ACA,ACG | T,T 2213 | XP_016863501.1 | |
XM_017008013.1 | 7108 | Silent Mutation | ACA,ACG | T,T 2212 | XP_016863502.1 | |
XM_017008014.1 | 7108 | Intron | XP_016863503.1 | |||
XM_017008015.1 | 7108 | Intron | XP_016863504.1 | |||
XM_017008016.1 | 7108 | Intron | XP_016863505.1 | |||
XM_017008017.1 | 7108 | Intron | XP_016863506.1 |
COX18 - COX18, cytochrome c oxidase assembly factor | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap Validated |