Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPSF7 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
CPSF7 - cleavage and polyadenylation specific factor 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136040.2 | 1420 | Silent Mutation | ATC,ATT | I,I 403 | NP_001129512.1 | |
NM_001142565.1 | 1420 | Silent Mutation | ATC,ATT | I,I 394 | NP_001136037.1 | |
NM_024811.3 | 1420 | Silent Mutation | ATC,ATT | I,I 446 | NP_079087.3 | |
XM_005274298.4 | 1420 | Silent Mutation | ATC,ATT | I,I 437 | XP_005274355.1 | |
XM_005274299.4 | 1420 | Silent Mutation | ATC,ATT | I,I 403 | XP_005274356.1 | |
XM_005274303.4 | 1420 | Silent Mutation | ATC,ATT | I,I 313 | XP_005274360.1 | |
XM_011545257.2 | 1420 | Silent Mutation | ATC,ATT | I,I 379 | XP_011543559.1 | |
XM_011545258.2 | 1420 | Silent Mutation | ATC,ATT | I,I 403 | XP_011543560.1 | |
XM_011545259.2 | 1420 | Silent Mutation | ATC,ATT | I,I 394 | XP_011543561.1 | |
XM_011545260.2 | 1420 | Silent Mutation | ATC,ATT | I,I 313 | XP_011543562.1 | |
XM_011545261.2 | 1420 | Silent Mutation | ATC,ATT | I,I 313 | XP_011543563.1 | |
XM_011545262.2 | 1420 | Silent Mutation | ATC,ATT | I,I 169 | XP_011543564.1 | |
XM_011545263.2 | 1420 | Silent Mutation | ATC,ATT | I,I 169 | XP_011543565.1 | |
XM_017018345.1 | 1420 | Silent Mutation | ATC,ATT | I,I 370 | XP_016873834.1 |
Set Membership: |
HapMap |