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TCTTGTTCTGATTCCAGCTCCAAAT[C/G]CAACTCCGACTCCTCTTCTACAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608480 | ||||||||||||||||||||
Literature Links: |
SLC26A8 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 |
SLC26A8 - solute carrier family 26 member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193476.1 | 2716 | Missense Mutation | CAT,GAT | H,D 861 | NP_001180405.1 | |
NM_052961.3 | 2716 | Missense Mutation | CAT,GAT | H,D 861 | NP_443193.1 | |
NM_138718.2 | 2716 | Missense Mutation | CAT,GAT | H,D 756 | NP_619732.2 | |
XM_011514294.2 | 2716 | Missense Mutation | CAT,GAT | H,D 835 | XP_011512596.1 | |
XM_017010235.1 | 2716 | Missense Mutation | CAT,GAT | H,D 861 | XP_016865724.1 |