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TTCCTGGGCCTTCCAGAGGAACTGC[A/G]CAGGCTGTCAGGCCTCTCCTCTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615903 MIM: 185261 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C22orf15 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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C22orf15 - chromosome 22 open reading frame 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182520.2 | 1123 | Missense Mutation | CAC,CGC | H,R 112 | NP_872326.2 | |
XM_011529907.2 | 1123 | Missense Mutation | CAC,CGC | H,R 182 | XP_011528209.1 | |
XM_011529908.2 | 1123 | Missense Mutation | CAC,CGC | H,R 117 | XP_011528210.2 | |
XM_011529912.2 | 1123 | Missense Mutation | CAC,CGC | H,R 129 | XP_011528214.1 | |
XM_017028602.1 | 1123 | Missense Mutation | CAC,CGC | H,R 210 | XP_016884091.1 | |
XM_017028603.1 | 1123 | Missense Mutation | CAC,CGC | H,R 203 | XP_016884092.1 | |
XM_017028604.1 | 1123 | Missense Mutation | CAC,CGC | H,R 190 | XP_016884093.1 | |
XM_017028605.1 | 1123 | Missense Mutation | CAC,CGC | H,R 187 | XP_016884094.1 | |
XM_017028606.1 | 1123 | Missense Mutation | CAC,CGC | H,R 210 | XP_016884095.1 | |
XM_017028607.1 | 1123 | Missense Mutation | CAC,CGC | H,R 210 | XP_016884096.1 | |
XM_017028608.1 | 1123 | Missense Mutation | CAC,CGC | H,R 210 | XP_016884097.1 | |
XM_017028609.1 | 1123 | Missense Mutation | CAC,CGC | H,R 147 | XP_016884098.1 | |
XM_017028610.1 | 1123 | Missense Mutation | CAC,CGC | H,R 140 | XP_016884099.1 | |
XM_017028611.1 | 1123 | Missense Mutation | ACA,GCA | T,A 184 | XP_016884100.1 | |
XM_017028612.1 | 1123 | Missense Mutation | CAC,CGC | H,R 112 | XP_016884101.1 | |
XM_017028613.1 | 1123 | Intron | XP_016884102.1 | |||
XM_017028614.1 | 1123 | Intron | XP_016884103.1 | |||
XM_017028615.1 | 1123 | Missense Mutation | ACA,GCA | T,A 114 | XP_016884104.1 | |
XM_017028616.1 | 1123 | Intron | XP_016884105.1 | |||
XM_017028617.1 | 1123 | Intron | XP_016884106.1 | |||
XM_017028618.1 | 1123 | Intron | XP_016884107.1 |
CHCHD10 - coiled-coil-helix-coiled-coil-helix domain containing 10 | ||||||
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There are no transcripts associated with this gene. |
MMP11 - matrix metallopeptidase 11 | ||||||
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There are no transcripts associated with this gene. |