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TGTGTTTATTGAACAGGTCAATAAT[G/T]TATGGCTGTGTAACGCTGATGAAGG
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 | |||
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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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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 | 907 | Missense Mutation | ATG,ATT | M,I 230 | NP_001036002.1 | |
NM_001177651.1 | 907 | Missense Mutation | ATG,ATT | M,I 178 | NP_001171122.1 | |
NM_006359.2 | 907 | Missense Mutation | ATG,ATT | M,I 198 | NP_006350.1 | |
XM_006724726.3 | 907 | Missense Mutation | ATG,ATT | M,I 178 | XP_006724789.1 | |
XM_011531243.2 | 907 | Missense Mutation | ATG,ATT | M,I 146 | XP_011529545.1 | |
XM_017029223.1 | 907 | Missense Mutation | ATG,ATT | M,I 178 | XP_016884712.1 | |
XM_017029224.1 | 907 | Missense Mutation | ATG,ATT | M,I 178 | XP_016884713.1 | |
XM_017029225.1 | 907 | Missense Mutation | ATG,ATT | M,I 146 | XP_016884714.1 |