Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCGGGCGGCGGGCGCACCATGCCC[A/T]CCTTCGACGAGGCGCTGCAGCGGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604842 | ||||||||||||||||||||
Literature Links: |
SLC22A3 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 |
SLC22A3 - solute carrier family 22 member 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021977.3 | 49 | Missense Mutation | ACC,TCC | T,S 3 | NP_068812.1 | |
XM_005267106.4 | 49 | Intron | XP_005267163.1 | |||
XM_005267107.3 | 49 | Missense Mutation | ACC,TCC | T,S 3 | XP_005267164.1 | |
XM_011536075.2 | 49 | Intron | XP_011534377.1 | |||
XM_011536076.2 | 49 | Intron | XP_011534378.1 | |||
XM_017011203.1 | 49 | Intron | XP_016866692.1 |