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Search Thermo Fisher Scientific
TGCCTCATTTGACAGAAAATTCGGC[A/G]GGAGATGACACGAACGAGCAAGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604334 MIM: 616463 | ||||||||||||||||||||
Literature Links: |
USP6 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 |
USP6 - ubiquitin specific peptidase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304284.1 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | NP_001291213.1 | |
NM_004505.3 | 2654 | Intron | NP_004496.2 | |||
XM_011524050.1 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522352.1 | |
XM_011524051.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522353.1 | |
XM_011524052.2 | 2654 | Intron | XP_011522354.1 | |||
XM_011524053.2 | 2654 | Intron | XP_011522355.1 | |||
XM_011524054.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522356.1 | |
XM_011524055.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522357.1 | |
XM_011524056.2 | 2654 | Intron | XP_011522358.1 | |||
XM_011524057.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522359.1 | |
XM_011524058.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522360.1 | |
XM_011524059.2 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_011522361.1 | |
XM_017025290.1 | 2654 | Missense Mutation | CAG,CGG | Q,R 69 | XP_016880779.1 |
ZNF232 - zinc finger protein 232 | ||||||
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There are no transcripts associated with this gene. |