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GCAGGATGTAGCATGTTCAGAGTCT[A/G]GTGACCTGAGCAGGCAGAGGAGGGG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610068 | |||||||||||||||||||||||
Literature Links: |
MIR6824 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 - 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 |
MIR6824 - microRNA 6824 | ||||||
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There are no transcripts associated with this gene. |
SLC26A6 - solute carrier family 26 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040454.1 | 2371 | Silent Mutation | ACC,ACT | T,T 736 | NP_001035544.1 | |
NM_001281732.1 | 2371 | Silent Mutation | ACC,ACT | T,T 721 | NP_001268661.1 | |
NM_001281733.1 | 2371 | Silent Mutation | ACC,ACT | T,T 649 | NP_001268662.1 | |
NM_022911.2 | 2371 | Silent Mutation | ACC,ACT | T,T 757 | NP_075062.2 | |
NM_134263.2 | 2371 | Silent Mutation | ACC,ACT | T,T 756 | NP_599025.2 | |
NM_134426.2 | 2371 | Silent Mutation | ACC,ACT | T,T 738 | NP_602298.2 |
TMEM89 - transmembrane protein 89 | ||||||
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There are no transcripts associated with this gene. |