Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCATGAAGTCTTCAAGACAGACAG[A/T]TAGGCTTTCACTGAGATCTTCGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
C22orf42 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
C22orf42 - chromosome 22 open reading frame 42 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010859.1 | 973 | Missense Mutation | ACT,TCT | T,S 175 | NP_001010859.1 | |
XM_011529922.2 | 973 | Intron | XP_011528224.1 | |||
XM_017028629.1 | 973 | Intron | XP_016884118.1 | |||
XM_017028630.1 | 973 | Missense Mutation | ACT,TCT | T,S 158 | XP_016884119.1 | |
XM_017028631.1 | 973 | UTR 3 | XP_016884120.1 | |||
XM_017028632.1 | 973 | Intron | XP_016884121.1 |