Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTCCTCTGCGGCCGGTTCCTCTG[C/T]GGCCTCCTCTGTGAGCTTCTCCTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300790 | ||||||||||||||||||||
Literature Links: |
CT47A12 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 |
CT47A12 - cancer/testis antigen family 47, member A12 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
CT47B1 - cancer/testis antigen family 47, member B1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145718.1 | 938 | Intron | NP_001139190.1 | |||
XM_017029734.1 | 938 | Missense Mutation | ACA,GCA | T,A 241 | XP_016885223.1 |