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CATATTCTGTGTCATGGAAAATTAT[C/G]GGATTTGTGTCCTTTTGTTCCTGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
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Literature Links: |
C1orf141 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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C1orf141 - chromosome 1 open reading frame 141 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276351.1 | 540 | Silent Mutation | CCC,CCG | P,P 208 | NP_001263280.1 | |
NM_001276352.1 | 540 | Missense Mutation | CCA,CGA | P,R 217 | NP_001263281.1 | |
XM_011541465.2 | 540 | Silent Mutation | CCC,CCG | P,P 279 | XP_011539767.1 | |
XM_011541466.2 | 540 | Silent Mutation | CCC,CCG | P,P 279 | XP_011539768.1 | |
XM_011541467.1 | 540 | Silent Mutation | CCC,CCG | P,P 266 | XP_011539769.1 | |
XM_011541469.1 | 540 | Silent Mutation | CCC,CCG | P,P 141 | XP_011539771.1 | |
XM_011541472.1 | 540 | Intron | XP_011539774.1 | |||
XM_011541473.2 | 540 | Missense Mutation | CCA,CGA | P,R 146 | XP_011539775.1 | |
XM_011541475.1 | 540 | Intron | XP_011539777.1 | |||
XM_017001276.1 | 540 | Silent Mutation | CCC,CCG | P,P 279 | XP_016856765.1 | |
XM_017001277.1 | 540 | Missense Mutation | CAT,GAT | H,D 240 | XP_016856766.1 |