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CTTGAGAATCTCCATCCCACTGGAC[C/T]CAAACATGAGGCCAGAGAAGTGTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607579 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SLC22A9 - solute carrier family 22 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_080866.2 | 509 | Missense Mutation | CCA,TCA | P,S 81 | NP_543142.2 | |
XM_017017159.1 | 509 | Missense Mutation | CCA,TCA | P,S 81 | XP_016872648.1 | |
XM_017017160.1 | 509 | UTR 5 | XP_016872649.1 |