Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTACCCTGTAAGAGCCGCCTCTATC[A/G]CCGCCCCCTGCCCCCGGCCCGCTGA
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 | |||||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | 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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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 |
UBXN2A - UBX domain protein 2A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181713.3 | Intron | NP_859064.2 | ||||
XM_005264166.4 | Intron | XP_005264223.1 | ||||
XM_005264167.4 | Intron | XP_005264224.1 | ||||
XM_005264168.4 | Intron | XP_005264225.1 | ||||
XM_005264169.4 | Intron | XP_005264226.1 | ||||
XM_011532633.2 | Intron | XP_011530935.1 | ||||
XM_017003517.1 | Intron | XP_016859006.1 | ||||
XM_017003518.1 | Intron | XP_016859007.1 |
Set Membership: |
HapMap Validated |