Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGCATGCTGGAGAACTTCTCGGC[C/T]GCCGTGCCCAGCCACCGCTGCTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 607096 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A12 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) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
SLC22A12 - solute carrier family 22 member 12 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276326.1 | 873 | Silent Mutation | GCC,GCT | A,A 42 | NP_001263255.1 | |
NM_001276327.1 | 873 | Silent Mutation | GCC,GCT | A,A 42 | NP_001263256.1 | |
NM_144585.3 | 873 | Silent Mutation | GCC,GCT | A,A 42 | NP_653186.2 | |
NM_153378.2 | 873 | UTR 5 | NP_700357.1 | |||
XM_006718430.3 | 873 | Silent Mutation | GCC,GCT | A,A 42 | XP_006718493.1 | |
XM_006718431.3 | 873 | Silent Mutation | GCC,GCT | A,A 7 | XP_006718494.1 |