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ACTTTGCTAAAGGCCTCTGAACCAG[A/G]GGCTGTCATAGCTTCAAAGTCGACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
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Literature Links: |
TTC13 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
TTC13 - tetratricopeptide repeat domain 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122835.2 | 3465 | Missense Mutation | CCT,TCT | P,S 752 | NP_001116307.2 | |
NM_024525.4 | 3465 | Missense Mutation | CCT,TCT | P,S 806 | NP_078801.3 | |
XM_005273260.1 | 3465 | Missense Mutation | CCT,TCT | P,S 805 | XP_005273317.1 | |
XM_005273261.2 | 3465 | Missense Mutation | CCT,TCT | P,S 775 | XP_005273318.1 | |
XM_005273262.1 | 3465 | Missense Mutation | CCT,TCT | P,S 753 | XP_005273319.1 | |
XM_005273264.2 | 3465 | Missense Mutation | CCT,TCT | P,S 730 | XP_005273321.1 | |
XM_006711814.2 | 3465 | Missense Mutation | CCT,TCT | P,S 727 | XP_006711877.1 | |
XM_006711815.2 | 3465 | Missense Mutation | CCT,TCT | P,S 448 | XP_006711878.1 | |
XM_011544275.2 | 3465 | Missense Mutation | CCT,TCT | P,S 699 | XP_011542577.1 | |
XM_011544276.2 | 3465 | Missense Mutation | CCT,TCT | P,S 509 | XP_011542578.1 | |
XM_017002321.1 | 3465 | Missense Mutation | CCT,TCT | P,S 774 | XP_016857810.1 | |
XM_017002322.1 | 3465 | Missense Mutation | CCT,TCT | P,S 729 | XP_016857811.1 | |
XM_017002323.1 | 3465 | Missense Mutation | CCT,TCT | P,S 677 | XP_016857812.1 | |
XM_017002324.1 | 3465 | Missense Mutation | CCT,TCT | P,S 676 | XP_016857813.1 | |
XM_017002325.1 | 3465 | Missense Mutation | CCT,TCT | P,S 447 | XP_016857814.1 | |
XM_017002326.1 | 3465 | Missense Mutation | CCT,TCT | P,S 447 | XP_016857815.1 |