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AATTGGGCATGAAAAACAAAATAAG[A/C]CTGTGAAAGCTGAATGACATTAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC91 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
|
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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CCDC91 - coiled-coil domain containing 91 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005253413.1 | Intron | XP_005253470.1 | ||||
XM_005253414.1 | Intron | XP_005253471.1 | ||||
XM_005253415.1 | Intron | XP_005253472.1 | ||||
XM_006719103.3 | Intron | XP_006719166.1 | ||||
XM_006719104.2 | Intron | XP_006719167.1 | ||||
XM_006719105.1 | Intron | XP_006719168.1 | ||||
XM_011520729.2 | Intron | XP_011519031.1 | ||||
XM_011520731.2 | Intron | XP_011519033.1 | ||||
XM_011520733.2 | Intron | XP_011519035.1 | ||||
XM_011520734.1 | Intron | XP_011519036.1 | ||||
XM_011520735.1 | Intron | XP_011519037.1 | ||||
XM_017019569.1 | Intron | XP_016875058.1 | ||||
XM_017019570.1 | Intron | XP_016875059.1 | ||||
XM_017019571.1 | Intron | XP_016875060.1 | ||||
XM_017019572.1 | Intron | XP_016875061.1 | ||||
XM_017019573.1 | Intron | XP_016875062.1 | ||||
XM_017019574.1 | Intron | XP_016875063.1 | ||||
XM_017019575.1 | Intron | XP_016875064.1 | ||||
XM_017019576.1 | Intron | XP_016875065.1 | ||||
XM_017019577.1 | Intron | XP_016875066.1 |
LOC729291 - translation initiation factor IF-2 | ||||||
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There are no transcripts associated with this gene. |