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CGATCCAGGTCTAGGTCCAGACCCA[A/G]CCCAGCCTCTTGTTCTGATTCCAGC
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 | |||
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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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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 | 2749 | Silent Mutation | CTG,TTG | L,L 872 | NP_001180405.1 | |
NM_052961.3 | 2749 | Silent Mutation | CTG,TTG | L,L 872 | NP_443193.1 | |
NM_138718.2 | 2749 | Silent Mutation | CTG,TTG | L,L 767 | NP_619732.2 | |
XM_011514294.2 | 2749 | Silent Mutation | CTG,TTG | L,L 846 | XP_011512596.1 | |
XM_017010235.1 | 2749 | Silent Mutation | CTG,TTG | L,L 872 | XP_016865724.1 |