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TTCTCCTCGGCCGCCCAGAACCTGC[A/G]AAGGGCCTACTCATTACAGCAGGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CFAP157 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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CFAP157 - cilia and flagella associated protein 157 | ||||||
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There are no transcripts associated with this gene. |
PTRH1 - peptidyl-tRNA hydrolase 1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002913.1 | 436 | Intron | NP_001002913.1 | |||
XM_006716955.3 | 436 | Intron | XP_006717018.1 | |||
XM_017014276.1 | 436 | Intron | XP_016869765.1 | |||
XM_017014277.1 | 436 | Intron | XP_016869766.1 | |||
XM_017014278.1 | 436 | Intron | XP_016869767.1 |
TTC16 - tetratricopeptide repeat domain 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317037.1 | 436 | Missense Mutation | CAA,CGA | Q,R 106 | NP_001303966.1 | |
NM_144965.2 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | NP_659402.1 | |
XM_005251733.1 | 436 | UTR 5 | XP_005251790.1 | |||
XM_005251734.1 | 436 | UTR 5 | XP_005251791.1 | |||
XM_006716970.1 | 436 | UTR 5 | XP_006717033.1 | |||
XM_006716971.1 | 436 | UTR 5 | XP_006717034.1 | |||
XM_011518283.1 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516585.1 | |
XM_011518284.1 | 436 | Intron | XP_011516586.1 | |||
XM_011518285.1 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516587.1 | |
XM_011518288.1 | 436 | Intron | XP_011516590.1 | |||
XM_011518289.2 | 436 | UTR 5 | XP_011516591.1 | |||
XM_011518290.1 | 436 | Intron | XP_011516592.1 | |||
XM_011518291.1 | 436 | UTR 5 | XP_011516593.1 | |||
XM_011518292.1 | 436 | Intron | XP_011516594.1 | |||
XM_011518293.1 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516595.1 | |
XM_011518294.2 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516596.1 | |
XM_011518295.1 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516597.1 | |
XM_011518297.1 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516599.1 | |
XM_011518298.2 | 436 | Missense Mutation | CAA,CGA | Q,R 119 | XP_011516600.1 |