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AATCCCAGCTCTGTCACCTTTAAGG[C/T]GCGTGACCCTGGGCTAATAACTACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608276 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
SLC22A16 - solute carrier family 22 member 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033125.3 | Intron | NP_149116.2 | ||||
XM_005267184.3 | Intron | XP_005267241.1 | ||||
XM_011536204.2 | Intron | XP_011534506.1 | ||||
XM_011536205.2 | Intron | XP_011534507.1 | ||||
XM_011536206.2 | Intron | XP_011534508.1 | ||||
XM_011536207.2 | Intron | XP_011534509.1 | ||||
XM_011536208.2 | Intron | XP_011534510.1 | ||||
XM_011536209.2 | Intron | XP_011534511.1 | ||||
XM_011536210.1 | Intron | XP_011534512.1 | ||||
XM_011536211.2 | Intron | XP_011534513.1 | ||||
XM_011536212.2 | Intron | XP_011534514.1 |