Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCTCACCTTCATCCTCCCCTGCC[C/T]CATGATACCTTCCCAGATGCTCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607097 | ||||||||||||||||||||
Literature Links: |
SLC22A11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
SLC22A11 - solute carrier family 22 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307985.1 | 485 | Missense Mutation | CCC,CTC | P,L 29 | NP_001294914.1 | |
NM_018484.3 | 485 | Missense Mutation | CCC,CTC | P,L 29 | NP_060954.1 | |
XM_011545167.1 | 485 | UTR 5 | XP_011543469.1 |