Search Thermo Fisher Scientific
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TGATTTTCTGCCACCGGAGTTTTGC[A/G]GACTTCGGGAAGATGGATGCATAAT
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
|
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Phenotype: |
MIM: 187020 | ||||||||||||||||||||||||||
Literature Links: |
TCP10 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EUR
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
EAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
SAS - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
AFR - Not Available | |||||
TCP10 - t-complex 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004610.3 | 668 | Intron | NP_004601.3 | |||
XM_011536082.2 | 668 | Intron | XP_011534384.1 | |||
XM_011536084.2 | 668 | Intron | XP_011534386.1 | |||
XM_011536085.2 | 668 | Intron | XP_011534387.1 | |||
XM_011536088.2 | 668 | Intron | XP_011534390.1 | |||
XM_011536090.2 | 668 | Intron | XP_011534392.1 | |||
XM_017011228.1 | 668 | Intron | XP_016866717.1 | |||
XM_017011229.1 | 668 | Intron | XP_016866718.1 | |||
XM_017011230.1 | 668 | Intron | XP_016866719.1 | |||
XM_017011231.1 | 668 | Missense Mutation | CCG,CTG | P,L 201 | XP_016866720.1 |