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CTTGTCCTTCTGTTTTTGGCTCACT[C/T]GTAAAAGCTGGAAGTCAAGGTGTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
28 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) - 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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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 | 2660 | UTR 3 | NP_443166.1 | |||
NM_134325.2 | 2660 | Missense Mutation | CAA,CGA | Q,R 849 | NP_599152.2 | |
XM_011509121.2 | 2660 | UTR 3 | XP_011507423.1 | |||
XM_011509122.2 | 2660 | UTR 3 | XP_011507424.1 | |||
XM_011509124.2 | 2660 | Intron | XP_011507426.1 |