Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCCTCAGCCACCGCTTCAATGAGA[C/T]GCAGCCTTGTGATATGGGCTGGGAA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||
Phenotype: |
MIM: 604047 | |||||||||||||||||||||||
Literature Links: |
SLC22A13 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SLC22A13 - solute carrier family 22 member 13 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004256.3 | 272 | Missense Mutation | ACG,ATG | T,M 106 | NP_004247.2 | |
XM_017007519.1 | 272 | UTR 5 | XP_016863008.1 |