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CTCCCAAACCTCCTGTGGACAGTAG[C/G]CTCCAGCGTCGGATGCAGACAACAG
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608147 | ||||||||||||||||||||||||||||||||
Literature Links: |
TUBGCP5 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
TUBGCP5 - tubulin gamma complex associated protein 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102610.1 | 3094 | Intron | NP_001096080.1 | |||
NM_052903.4 | 3094 | Intron | NP_443135.3 | |||
XM_005272540.2 | 3094 | Intron | XP_005272597.1 | |||
XM_011543868.1 | 3094 | Silent Mutation | AGC,AGG | S,R 1024 | XP_011542170.1 | |
XM_011543869.2 | 3094 | Silent Mutation | AGC,AGG | S,R 1023 | XP_011542171.1 | |
XM_011543870.1 | 3094 | Silent Mutation | AGC,AGG | S,R 1021 | XP_011542172.1 | |
XM_017021890.1 | 3094 | Intron | XP_016877379.1 | |||
XM_017021891.1 | 3094 | Intron | XP_016877380.1 | |||
XM_017021892.1 | 3094 | Silent Mutation | AGC,AGG | S,R 1020 | XP_016877381.1 | |
XM_017021893.1 | 3094 | Intron | XP_016877382.1 | |||
XM_017021894.1 | 3094 | Intron | XP_016877383.1 | |||
XM_017021895.1 | 3094 | Intron | XP_016877384.1 | |||
XM_017021896.1 | 3094 | Intron | XP_016877385.1 | |||
XM_017021897.1 | 3094 | Intron | XP_016877386.1 | |||
XM_017021898.1 | 3094 | Intron | XP_016877387.1 | |||
XM_017021899.1 | 3094 | Intron | XP_016877388.1 | |||
XM_017021900.1 | 3094 | Intron | XP_016877389.1 | |||
XM_017021901.1 | 3094 | Intron | XP_016877390.1 |
Set Membership: |
HapMap |