Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCTCTCTGGATCGGTGATTTCTG[A/T]TAAAAGACCTGCAAAGCACAACGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
9 submissions
|
||||||||||||||||||||
Phenotype: |
MIM: 609890 | ||||||||||||||||||||
Literature Links: |
UBR4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
UBR4 - ubiquitin protein ligase E3 component n-recognin 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020765.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5166 | NP_065816.2 | |
XM_011541108.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5217 | XP_011539410.1 | |
XM_011541109.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5216 | XP_011539411.1 | |
XM_011541110.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5216 | XP_011539412.1 | |
XM_011541111.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5216 | XP_011539413.1 | |
XM_011541112.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5212 | XP_011539414.1 | |
XM_011541113.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5211 | XP_011539415.1 | |
XM_011541114.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5211 | XP_011539416.1 | |
XM_011541115.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5209 | XP_011539417.1 | |
XM_011541116.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5206 | XP_011539418.1 | |
XM_011541117.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5189 | XP_011539419.1 | |
XM_011541118.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5188 | XP_011539420.1 | |
XM_011541119.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5177 | XP_011539421.1 | |
XM_011541120.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5176 | XP_011539422.1 | |
XM_011541121.2 | 15477 | Missense Mutation | ACA,TCA | T,S 5165 | XP_011539423.1 | |
XM_017000822.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5210 | XP_016856311.1 | |
XM_017000823.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5201 | XP_016856312.1 | |
XM_017000824.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5183 | XP_016856313.1 | |
XM_017000825.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5178 | XP_016856314.1 | |
XM_017000826.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5177 | XP_016856315.1 | |
XM_017000827.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5172 | XP_016856316.1 | |
XM_017000828.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5164 | XP_016856317.1 | |
XM_017000829.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5148 | XP_016856318.1 | |
XM_017000830.1 | 15477 | Missense Mutation | ACA,TCA | T,S 5131 | XP_016856319.1 |