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AGCACATCCATATACTTTTTTCCTT[G/T]TTTAAACAATGATCTAAGAGACCCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
22 submissions
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Phenotype: |
MIM: 600278 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAP1GAP 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)
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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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RAP1GAP - RAP1 GTPase activating protein | ||||||
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There are no transcripts associated with this gene. |
USP48 - ubiquitin specific peptidase 48 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001032730.1 | Intron | NP_001027902.1 | ||||
XM_005246009.2 | Intron | XP_005246066.1 | ||||
XM_006710951.2 | Intron | XP_006711014.2 | ||||
XM_006710955.3 | Intron | XP_006711018.1 | ||||
XM_011542262.2 | Intron | XP_011540564.1 | ||||
XM_011542263.2 | Intron | XP_011540565.1 | ||||
XM_011542264.1 | Intron | XP_011540566.1 | ||||
XM_011542265.2 | Intron | XP_011540567.1 | ||||
XM_011542267.2 | Intron | XP_011540569.1 | ||||
XM_011542268.2 | Intron | XP_011540570.1 | ||||
XM_017002495.1 | Intron | XP_016857984.1 | ||||
XM_017002496.1 | Intron | XP_016857985.1 | ||||
XM_017002497.1 | Intron | XP_016857986.1 |
Set Membership: |
HapMap |