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- SNP ID:
- rs775887467
- Gene
-
USP33 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 77740811 - 77740811 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TACAACTTGAATTAATAATGTTATA[C/T]TGGCTTTCCCTTTCCTTCAGGCACT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
|
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Phenotype: |
MIM: 615146
|
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Literature Links: |
USP33 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 |
| USP33 - ubiquitin specific peptidase 33 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015017.4 | Intron | NP_055832.3 | ||||
| NM_201624.2 | Intron | NP_963918.1 | ||||
| NM_201626.2 | Intron | NP_963920.1 | ||||
| XM_005270648.1 | Intron | XP_005270705.1 | ||||
| XM_005270649.1 | Intron | XP_005270706.1 | ||||
| XM_011541055.1 | Intron | XP_011539357.1 | ||||
| XM_011541056.2 | Intron | XP_011539358.1 | ||||
| XM_017000722.1 | Intron | XP_016856211.1 | ||||
| XM_017000723.1 | Intron | XP_016856212.1 | ||||
| XM_017000724.1 | Intron | XP_016856213.1 | ||||
| XM_017000725.1 | Intron | XP_016856214.1 | ||||
| XM_017000726.1 | Intron | XP_016856215.1 | ||||
| XM_017000727.1 | Intron | XP_016856216.1 | ||||
| XM_017000728.1 | Intron | XP_016856217.1 | ||||
| XM_017000729.1 | Intron | XP_016856218.1 | ||||
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