Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAACACTTACCAGAGATGATGCCG[A/G]TGGCGACGTACATATGAGAAACCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610008 MIM: 603880 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARSG 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SLC16A6 - solute carrier family 16 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174166.1 | 675 | Missense Mutation | ACC,ATC | T,I 121 | NP_001167637.1 | |
NM_004694.4 | 675 | Missense Mutation | ACC,ATC | T,I 121 | NP_004685.2 | |
XM_005257789.3 | 675 | Missense Mutation | ACC,ATC | T,I 125 | XP_005257846.2 | |
XM_011525461.2 | 675 | Missense Mutation | ACC,ATC | T,I 121 | XP_011523763.1 | |
XM_017025291.1 | 675 | Missense Mutation | ACC,ATC | T,I 121 | XP_016880780.1 | |
XM_017025292.1 | 675 | Missense Mutation | ACC,ATC | T,I 121 | XP_016880781.1 |
Set Membership: |
HapMap |