Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCAATCTTAGTATTGTCAATAGG[A/C]CCTGGAGGATCTAAAGGAAAAAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
|
||||||||||||||||||||
Phenotype: |
MIM: 615146 | ||||||||||||||||||||
Literature Links: |
USP33 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 |
USP33 - ubiquitin specific peptidase 33 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015017.4 | 2987 | Silent Mutation | GGG,GGT | G,G 871 | NP_055832.3 | |
NM_201624.2 | 2987 | Silent Mutation | GGG,GGT | G,G 840 | NP_963918.1 | |
NM_201626.2 | 2987 | Intron | NP_963920.1 | |||
XM_005270648.1 | 2987 | Silent Mutation | GGG,GGT | G,G 863 | XP_005270705.1 | |
XM_005270649.1 | 2987 | Missense Mutation | GGC,GTC | G,V 837 | XP_005270706.1 | |
XM_011541055.1 | 2987 | Silent Mutation | GGG,GGT | G,G 772 | XP_011539357.1 | |
XM_011541056.2 | 2987 | Intron | XP_011539358.1 | |||
XM_017000722.1 | 2987 | Silent Mutation | GGG,GGT | G,G 832 | XP_016856211.1 | |
XM_017000723.1 | 2987 | Missense Mutation | GGC,GTC | G,V 806 | XP_016856212.1 | |
XM_017000724.1 | 2987 | Missense Mutation | GGC,GTC | G,V 798 | XP_016856213.1 | |
XM_017000725.1 | 2987 | Silent Mutation | GGG,GGT | G,G 741 | XP_016856214.1 | |
XM_017000726.1 | 2987 | Silent Mutation | GGG,GGT | G,G 733 | XP_016856215.1 | |
XM_017000727.1 | 2987 | Silent Mutation | GGG,GGT | G,G 692 | XP_016856216.1 | |
XM_017000728.1 | 2987 | Silent Mutation | GGG,GGT | G,G 692 | XP_016856217.1 | |
XM_017000729.1 | 2987 | Missense Mutation | GGC,GTC | G,V 738 | XP_016856218.1 |