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TACACCGTTTTCTGCCTCGGCAGCG[A/G]CAGCATGTCTGAGAGACAAGACAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604725 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
USP2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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USP2 - ubiquitin specific peptidase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243759.1 | 687 | Silent Mutation | TGC,TGT | C,C 234 | NP_001230688.1 | |
NM_004205.4 | 687 | Silent Mutation | TGC,TGT | C,C 477 | NP_004196.4 | |
NM_171997.2 | 687 | Silent Mutation | TGC,TGT | C,C 268 | NP_741994.1 | |
XM_005271721.4 | 687 | Silent Mutation | TGC,TGT | C,C 477 | XP_005271778.1 | |
XM_005271722.2 | 687 | Silent Mutation | TGC,TGT | C,C 477 | XP_005271779.1 | |
XM_017018539.1 | 687 | Silent Mutation | TGC,TGT | C,C 224 | XP_016874028.1 |