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GACATGGCCTCCACCCGCTATGAGT[C/T]CCTATTGGAGAACCTGGATGACCAT
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1376 | Missense Mutation | TCC,TTC | S,F 95 | NP_872326.2 | |
XM_011529907.2 | 1376 | Missense Mutation | TCC,TTC | S,F 165 | XP_011528209.1 | |
XM_011529908.2 | 1376 | Missense Mutation | TCC,TTC | S,F 100 | XP_011528210.2 | |
XM_011529912.2 | 1376 | Missense Mutation | TCC,TTC | S,F 112 | XP_011528214.1 | |
XM_017028602.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884091.1 | |
XM_017028603.1 | 1376 | Missense Mutation | CCC,TCC | P,S 160 | XP_016884092.1 | |
XM_017028604.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884093.1 | |
XM_017028605.1 | 1376 | Missense Mutation | TCC,TTC | S,F 170 | XP_016884094.1 | |
XM_017028606.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884095.1 | |
XM_017028607.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884096.1 | |
XM_017028608.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884097.1 | |
XM_017028609.1 | 1376 | Missense Mutation | CCC,TCC | P,S 104 | XP_016884098.1 | |
XM_017028610.1 | 1376 | Missense Mutation | CCC,TCC | P,S 97 | XP_016884099.1 | |
XM_017028611.1 | 1376 | Missense Mutation | CCC,TCC | P,S 167 | XP_016884100.1 | |
XM_017028612.1 | 1376 | Missense Mutation | TCC,TTC | S,F 95 | XP_016884101.1 | |
XM_017028613.1 | 1376 | Missense Mutation | TCC,TTC | S,F 170 | XP_016884102.1 | |
XM_017028614.1 | 1376 | Missense Mutation | TCC,TTC | S,F 165 | XP_016884103.1 | |
XM_017028615.1 | 1376 | Missense Mutation | CCC,TCC | P,S 97 | XP_016884104.1 | |
XM_017028616.1 | 1376 | Missense Mutation | TCC,TTC | S,F 100 | XP_016884105.1 | |
XM_017028617.1 | 1376 | Missense Mutation | CCC,TCC | P,S 97 | XP_016884106.1 | |
XM_017028618.1 | 1376 | 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. |