Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C22orf42 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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C22orf42 - chromosome 22 open reading frame 42 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010859.1 | 761 | Missense Mutation | CCG,CTG | P,L 73 | NP_001010859.1 | |
XM_011529922.2 | 761 | Intron | XP_011528224.1 | |||
XM_017028629.1 | 761 | Intron | XP_016884118.1 | |||
XM_017028630.1 | 761 | Missense Mutation | CCG,CTG | P,L 87 | XP_016884119.1 | |
XM_017028631.1 | 761 | Missense Mutation | CCG,CTG | P,L 87 | XP_016884120.1 | |
XM_017028632.1 | 761 | Intron | XP_016884121.1 |
Set Membership: |
HapMap |