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AAGTAAGCTAGATCTGATTCTATAA[C/T]AACCTTACAAAACAACAAATTTACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615867 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBC1D32 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TBC1D32 - TBC1 domain family member 32 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152730.5 | 4226 | UTR 3 | NP_689943.4 | |||
XM_005266861.2 | 4226 | UTR 3 | XP_005266918.1 | |||
XM_011535569.1 | 4226 | UTR 3 | XP_011533871.1 | |||
XM_011535570.1 | 4226 | UTR 3 | XP_011533872.1 | |||
XM_011535571.2 | 4226 | UTR 3 | XP_011533873.1 | |||
XM_011535574.1 | 4226 | UTR 3 | XP_011533876.1 | |||
XM_011535575.2 | 4226 | Intron | XP_011533877.1 | |||
XM_011535576.2 | 4226 | Intron | XP_011533878.1 | |||
XM_011535580.2 | 4226 | UTR 3 | XP_011533882.1 | |||
XM_011535582.2 | 4226 | Intron | XP_011533884.1 | |||
XM_011535585.2 | 4226 | Intron | XP_011533887.1 | |||
XM_017010397.1 | 4226 | UTR 3 | XP_016865886.1 | |||
XM_017010398.1 | 4226 | UTR 3 | XP_016865887.1 | |||
XM_017010399.1 | 4226 | UTR 3 | XP_016865888.1 | |||
XM_017010400.1 | 4226 | UTR 3 | XP_016865889.1 | |||
XM_017010401.1 | 4226 | UTR 3 | XP_016865890.1 | |||
XM_017010402.1 | 4226 | Intron | XP_016865891.1 | |||
XM_017010403.1 | 4226 | Intron | XP_016865892.1 | |||
XM_017010404.1 | 4226 | UTR 3 | XP_016865893.1 | |||
XM_017010405.1 | 4226 | Intron | XP_016865894.1 |