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CCCCACTTAGGCCAAGTCCTGCTCC[A/G]TCTCGCCCAGGCTGAAGGACCAATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C11orf42 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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C11orf42 - chromosome 11 open reading frame 42 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173525.2 | 2998 | Intron | NP_775796.2 | |||
XM_011519926.2 | 2998 | Intron | XP_011518228.1 | |||
XM_011519927.2 | 2998 | Intron | XP_011518229.1 |
FAM160A2 - family with sequence similarity 160 member A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098794.1 | 2998 | Silent Mutation | GAC,GAT | D,D 887 | NP_001092264.1 | |
NM_032127.3 | 2998 | Silent Mutation | GAC,GAT | D,D 901 | NP_115503.2 | |
XM_006718343.2 | 2998 | Silent Mutation | GAC,GAT | D,D 901 | XP_006718406.1 | |
XM_011520397.2 | 2998 | Silent Mutation | GAC,GAT | D,D 901 | XP_011518699.1 | |
XM_011520398.2 | 2998 | Intron | XP_011518700.1 | |||
XM_011520399.2 | 2998 | Intron | XP_011518701.1 |