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GAGGGCCATTAAATATGGGTCCTCC[A/G]GCACCATCAGGGATAGGTGCTACTG
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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | 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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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 | 7030 | Silent Mutation | GCC,GCT | A,A 2438 | NP_001273700.1 | |
NM_015574.1 | 7030 | Silent Mutation | GCC,GCT | A,A 2550 | NP_056389.1 | |
NM_032217.4 | 7030 | Silent Mutation | GCC,GCT | A,A 2551 | NP_115593.3 | |
NM_198889.2 | 7030 | Silent Mutation | GCC,GCT | A,A 2300 | NP_942592.1 | |
XM_005265671.3 | 7030 | Silent Mutation | GCC,GCT | A,A 2299 | XP_005265728.1 | |
XM_005265672.3 | 7030 | Intron | XP_005265729.1 | |||
XM_005265673.3 | 7030 | Intron | XP_005265730.1 | |||
XM_017008011.1 | 7030 | Silent Mutation | GCC,GCT | A,A 2437 | XP_016863500.1 | |
XM_017008012.1 | 7030 | Silent Mutation | GCC,GCT | A,A 2187 | XP_016863501.1 | |
XM_017008013.1 | 7030 | Silent Mutation | GCC,GCT | A,A 2186 | XP_016863502.1 | |
XM_017008014.1 | 7030 | Intron | XP_016863503.1 | |||
XM_017008015.1 | 7030 | Intron | XP_016863504.1 | |||
XM_017008016.1 | 7030 | Intron | XP_016863505.1 | |||
XM_017008017.1 | 7030 | Intron | XP_016863506.1 |
COX18 - COX18, cytochrome c oxidase assembly factor | ||||||
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There are no transcripts associated with this gene. |