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TTCGATGATATCTTCAAAGATATGA[A/G]TAAGTCTACCTACTTGTTCCATTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300395 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
THOC2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
THOC2 - THO complex 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001081550.1 | Intron | NP_001075019.1 | ||||
XM_005262450.3 | Intron | XP_005262507.1 | ||||
XM_017029662.1 | Intron | XP_016885151.1 | ||||
XM_017029663.1 | Intron | XP_016885152.1 | ||||
XM_017029664.1 | Intron | XP_016885153.1 | ||||
XM_017029665.1 | Intron | XP_016885154.1 | ||||
XM_017029666.1 | Intron | XP_016885155.1 | ||||
XM_017029667.1 | Intron | XP_016885156.1 | ||||
XM_017029668.1 | Intron | XP_016885157.1 | ||||
XM_017029669.1 | Intron | XP_016885158.1 | ||||
XM_017029670.1 | Intron | XP_016885159.1 | ||||
XM_017029671.1 | Intron | XP_016885160.1 | ||||
XM_017029672.1 | Intron | XP_016885161.1 | ||||
XM_017029673.1 | Intron | XP_016885162.1 | ||||
XM_017029674.1 | Intron | XP_016885163.1 | ||||
XM_017029675.1 | Intron | XP_016885164.1 | ||||
XM_017029676.1 | Intron | XP_016885165.1 | ||||
XM_017029677.1 | Intron | XP_016885166.1 | ||||
XM_017029678.1 | Intron | XP_016885167.1 | ||||
XM_017029679.1 | Intron | XP_016885168.1 |