Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACAGTGGCAGCTCTTGGACCCCA[A/G]TGCCACGGCCACCAGCTGGAGCGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 607096 | ||||||||||||||||||||
Literature Links: |
SLC22A12 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 |
SLC22A12 - solute carrier family 22 member 12 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276326.1 | 1052 | Missense Mutation | AAT,AGT | N,S 102 | NP_001263255.1 | |
NM_001276327.1 | 1052 | Missense Mutation | AAT,AGT | N,S 102 | NP_001263256.1 | |
NM_144585.3 | 1052 | Missense Mutation | AAT,AGT | N,S 102 | NP_653186.2 | |
NM_153378.2 | 1052 | UTR 5 | NP_700357.1 | |||
XM_006718430.3 | 1052 | Missense Mutation | AAT,AGT | N,S 102 | XP_006718493.1 | |
XM_006718431.3 | 1052 | Missense Mutation | AAT,AGT | N,S 67 | XP_006718494.1 |