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CCCTGCTCCCCCCAGTTCCCCAGCC[C/T]GACGCACACTCTACACGCAGGCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615347 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATAD2B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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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ATAD2B - ATPase family, AAA domain containing 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242338.2 | Intron | NP_001229267.2 | ||||
NM_017552.3 | Intron | NP_060022.2 | ||||
XM_005264372.3 | Intron | XP_005264429.2 | ||||
XM_006712030.3 | Intron | XP_006712093.1 | ||||
XM_006712031.3 | Intron | XP_006712094.1 | ||||
XM_011532918.2 | Intron | XP_011531220.1 | ||||
XM_011532919.2 | Intron | XP_011531221.1 | ||||
XM_011532920.2 | Intron | XP_011531222.1 | ||||
XM_011532921.2 | Intron | XP_011531223.1 | ||||
XM_011532924.2 | Intron | XP_011531226.1 | ||||
XM_011532925.2 | Intron | XP_011531227.1 | ||||
XM_011532928.1 | Intron | XP_011531230.1 | ||||
XM_011532929.2 | Intron | XP_011531231.1 | ||||
XM_011532930.2 | Intron | XP_011531232.1 | ||||
XM_011532931.2 | Intron | XP_011531233.1 | ||||
XM_011532932.1 | Intron | XP_011531234.1 | ||||
XM_017004375.1 | Intron | XP_016859864.1 |
KLHL29 - kelch like family member 29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052920.1 | Intron | NP_443152.1 | ||||
XM_006711929.3 | Intron | XP_006711992.1 | ||||
XM_011532501.2 | Intron | XP_011530803.1 | ||||
XM_017003264.1 | Intron | XP_016858753.1 |