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GATGTGTGTATGTACGTGTGGATCT[A/G]TGCAATCCACAAGATGTAAAGCTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616010 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COPS7B 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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COPS7B - COP9 signalosome subunit 7B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282949.2 | Intron | NP_001269878.1 | ||||
NM_001282950.2 | Intron | NP_001269879.1 | ||||
NM_001282951.2 | Intron | NP_001269880.1 | ||||
NM_001282952.2 | Intron | NP_001269881.1 | ||||
NM_001308381.1 | Intron | NP_001295310.1 | ||||
NM_022730.3 | Intron | NP_073567.1 | ||||
XM_006712693.1 | Intron | XP_006712756.1 | ||||
XM_011511638.1 | Intron | XP_011509940.1 | ||||
XM_011511639.1 | Intron | XP_011509941.1 | ||||
XM_011511640.1 | Intron | XP_011509942.1 | ||||
XM_017004716.1 | Intron | XP_016860205.1 | ||||
XM_017004717.1 | Intron | XP_016860206.1 |