Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAAGAGCATATACCTGCAATATCTT[A/G]CCCAAGGTAAGAGCACCAATGGTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610748 | ||||||||||||||||||||
Literature Links: |
USP28 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
USP28 - ubiquitin specific peptidase 28 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301029.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 859 | NP_001287958.1 | |
NM_020886.3 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1016 | NP_065937.1 | |
XM_005271630.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1079 | XP_005271687.1 | |
XM_005271631.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1078 | XP_005271688.1 | |
XM_005271632.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1076 | XP_005271689.1 | |
XM_005271633.4 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1057 | XP_005271690.1 | |
XM_005271636.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1019 | XP_005271693.1 | |
XM_005271637.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1017 | XP_005271694.1 | |
XM_005271638.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 985 | XP_005271695.1 | |
XM_005271639.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 984 | XP_005271696.1 | |
XM_011542936.2 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1053 | XP_011541238.1 | |
XM_011542938.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 954 | XP_011541240.1 | |
XM_011542941.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 726 | XP_011541243.1 | |
XM_011542942.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 635 | XP_011541244.1 | |
XM_017018056.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1052 | XP_016873545.1 | |
XM_017018057.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 1013 | XP_016873546.1 | |
XM_017018058.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 990 | XP_016873547.1 | |
XM_017018059.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 958 | XP_016873548.1 | |
XM_017018060.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 953 | XP_016873549.1 | |
XM_017018061.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 892 | XP_016873550.1 | |
XM_017018062.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 891 | XP_016873551.1 | |
XM_017018063.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 791 | XP_016873552.1 | |
XM_017018064.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 729 | XP_016873553.1 | |
XM_017018065.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 664 | XP_016873554.1 | |
XM_017018066.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 664 | XP_016873555.1 | |
XM_017018067.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 664 | XP_016873556.1 | |
XM_017018068.1 | 3300 | Nonsense Mutation | CAA,TAA | Q,* 632 | XP_016873557.1 | |
XM_017018069.1 | 3300 | Intron | XP_016873558.1 |