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GGAGGACTTCCACCTTTGCCTACAG[A/G]AGGACCCCATTGTGTCTCTGGGCCA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
31 submissions
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Phenotype: |
MIM: 608481 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC26A9 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)
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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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SLC26A9 - solute carrier family 26 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052934.3 | 3407 | UTR 3 | NP_443166.1 | |||
NM_134325.2 | 3407 | UTR 3 | NP_599152.2 | |||
XM_011509121.2 | 3407 | UTR 3 | XP_011507423.1 | |||
XM_011509122.2 | 3407 | UTR 3 | XP_011507424.1 | |||
XM_011509124.2 | 3407 | Intron | XP_011507426.1 |
Set Membership: |
HapMap |