Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C17orf80 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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C17orf80 - chromosome 17 open reading frame 80 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100621.2 | 1809 | Silent Mutation | ACG,ACT | T,T 522 | NP_001094091.1 | |
NM_001100622.2 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | NP_001094092.1 | |
NM_001288770.1 | 1809 | Silent Mutation | ACG,ACT | T,T 522 | NP_001275699.1 | |
NM_001288771.1 | 1809 | Silent Mutation | ACG,ACT | T,T 522 | NP_001275700.1 | |
NM_017941.5 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | NP_060411.2 | |
XM_005257487.3 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | XP_005257544.1 | |
XM_006721966.3 | 1809 | Silent Mutation | ACG,ACT | T,T 522 | XP_006722029.1 | |
XM_011524961.1 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | XP_011523263.1 | |
XM_011524962.2 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | XP_011523264.1 | |
XM_017024806.1 | 1809 | Silent Mutation | ACG,ACT | T,T 558 | XP_016880295.1 |
CPSF4L - cleavage and polyadenylation specific factor 4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001129885.1 | 1809 | Intron | NP_001123357.1 | |||
XM_011525115.2 | 1809 | Intron | XP_011523417.1 |
Set Membership: |
HapMap Validated |