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CCAGTACCTGGTGCTGTAGTTTATT[C/T]GAGTTCATCTGTACCTGATAAATCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
USP42 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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USP42 - ubiquitin specific peptidase 42 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032172.2 | 256 | Missense Mutation | TCG,TTG | S,L 64 | NP_115548.1 | |
XM_005249883.4 | 256 | Missense Mutation | TCG,TTG | S,L 64 | XP_005249940.1 | |
XM_006715790.1 | 256 | Missense Mutation | TCG,TTG | S,L 64 | XP_006715853.1 | |
XM_006715791.2 | 256 | Missense Mutation | TCG,TTG | S,L 64 | XP_006715854.1 | |
XM_011515573.1 | 256 | Missense Mutation | TCG,TTG | S,L 64 | XP_011513875.1 | |
XM_011515574.1 | 256 | UTR 5 | XP_011513876.1 | |||
XM_011515577.1 | 256 | Intron | XP_011513879.1 | |||
XM_011515578.1 | 256 | UTR 5 | XP_011513880.1 |