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CCTTTGCTAAAGCTGATACAGAATG[C/G]ACTTTCTTCTTATTGTTTACAATAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601387 MIM: 610985 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TSG101 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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TSG101 - tumor susceptibility 101 | ||||||
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There are no transcripts associated with this gene. |
UEVLD - UEV and lactate/malate dehyrogenase domains | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040697.2 | 3147 | Silent Mutation | GTC,GTG | V,V 408 | NP_001035787.1 | |
NM_001261382.1 | 3147 | Silent Mutation | GTC,GTG | V,V 386 | NP_001248311.1 | |
NM_001261383.1 | 3147 | Intron | NP_001248312.1 | |||
NM_001261384.1 | 3147 | Silent Mutation | GTC,GTG | V,V 278 | NP_001248313.1 | |
NM_001261385.1 | 3147 | Intron | NP_001248314.1 | |||
NM_001261386.1 | 3147 | Intron | NP_001248315.1 | |||
NM_001297771.1 | 3147 | Intron | NP_001284700.1 | |||
NM_018314.4 | 3147 | Intron | NP_060784.3 | |||
XM_006718255.2 | 3147 | Silent Mutation | GTC,GTG | V,V 185 | XP_006718318.1 | |
XM_011520201.2 | 3147 | Silent Mutation | GTC,GTG | V,V 185 | XP_011518503.1 | |
XM_017017985.1 | 3147 | Silent Mutation | GTC,GTG | V,V 278 | XP_016873474.1 | |
XM_017017986.1 | 3147 | Intron | XP_016873475.1 |