Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCATCTGAAAATCTCGAAGCCACG[C/T]AGAAGATACTTTCATCTCTGAAGAG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||||||||||||||||||||
Phenotype: |
||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CXorf38 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
CXorf38 - chromosome X open reading frame 38 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144970.2 | 573 | Missense Mutation | ACG,GCG | T,A 176 | NP_659407.1 | |
XM_005272589.2 | 573 | Missense Mutation | ACG,GCG | T,A 176 | XP_005272646.2 | |
XM_006724527.3 | 573 | Missense Mutation | ACG,GCG | T,A 176 | XP_006724590.2 | |
XM_006724528.2 | 573 | Missense Mutation | ACG,GCG | T,A 131 | XP_006724591.1 | |
XM_017029302.1 | 573 | Missense Mutation | ACG,GCG | T,A 187 | XP_016884791.1 | |
XM_017029303.1 | 573 | Missense Mutation | ACG,GCG | T,A 131 | XP_016884792.1 | |
XM_017029304.1 | 573 | Missense Mutation | ACG,GCG | T,A 57 | XP_016884793.1 | |
XM_017029305.1 | 573 | Missense Mutation | ACG,GCG | T,A 57 | XP_016884794.1 |