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GGGCAGGGGCTTCGGACGGCGGCGG[C/T]GGAGAGGCTAGAGCCATGGACGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300231 | ||||||||||||||||||||
Literature Links: |
SLC9A6 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 |
SLC9A6 - solute carrier family 9 member A6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042537.1 | 358 | Silent Mutation | GGC,GGT | G,G 47 | NP_001036002.1 | |
NM_001177651.1 | 358 | UTR 5 | NP_001171122.1 | |||
NM_006359.2 | 358 | Silent Mutation | GGC,GGT | G,G 47 | NP_006350.1 | |
XM_006724726.3 | 358 | UTR 5 | XP_006724789.1 | |||
XM_011531243.2 | 358 | UTR 5 | XP_011529545.1 | |||
XM_017029223.1 | 358 | UTR 5 | XP_016884712.1 | |||
XM_017029224.1 | 358 | UTR 5 | XP_016884713.1 | |||
XM_017029225.1 | 358 | UTR 5 | XP_016884714.1 |