Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGAGGAGCCTGGGTTCAGGGACT[C/T]AGTGTGAGGCTCCATGACAGTCACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 609577 MIM: 613475 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUL7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
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
|
|||||
AMR
|
CUL7 - cullin 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168370.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1742 | NP_001161842.1 | |
NM_014780.4 | 5348 | Missense Mutation | AAG,GAG | K,E 1658 | NP_055595.2 | |
XM_005249503.2 | 5348 | Missense Mutation | AAG,GAG | K,E 1710 | XP_005249560.1 | |
XM_006715285.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1694 | XP_006715348.1 | |
XM_011515019.2 | 5348 | Missense Mutation | AAG,GAG | K,E 1746 | XP_011513321.1 | |
XM_011515020.2 | 5348 | Missense Mutation | AAG,GAG | K,E 1714 | XP_011513322.1 | |
XM_011515021.1 | 5348 | Missense Mutation | AAG,GAG | K,E 949 | XP_011513323.1 | |
XM_017011533.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1755 | XP_016867022.1 | |
XM_017011534.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1751 | XP_016867023.1 | |
XM_017011535.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1723 | XP_016867024.1 | |
XM_017011536.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1703 | XP_016867025.1 | |
XM_017011537.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1690 | XP_016867026.1 | |
XM_017011538.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1671 | XP_016867027.1 | |
XM_017011539.1 | 5348 | Missense Mutation | AAG,GAG | K,E 1662 | XP_016867028.1 | |
XM_017011540.1 | 5348 | Intron | XP_016867029.1 |
RRP36 - ribosomal RNA processing 36 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |