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GGGCAAGATGGCGGCGGCAGTAGGG[G/T]TTCGTGGCCGGTACGAGCTGCCGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TTC17 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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TTC17 - tetratricopeptide repeat domain 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307943.1 | 89 | Missense Mutation | GTT,TTT | V,F 7 | NP_001294872.1 | |
NM_018259.5 | 89 | Missense Mutation | GTT,TTT | V,F 7 | NP_060729.2 | |
XM_005253016.1 | 89 | Missense Mutation | GTT,TTT | V,F 7 | XP_005253073.1 | |
XM_006718263.1 | 89 | Intron | XP_006718326.1 | |||
XM_011520218.2 | 89 | Missense Mutation | GTT,TTT | V,F 7 | XP_011518520.1 | |
XM_017018010.1 | 89 | Missense Mutation | GTT,TTT | V,F 7 | XP_016873499.1 |