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CAAATACAGCAAAAGAGAAATTATC[A/G]TCATCTTTGGTGAAGATCAAACAAA
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) - 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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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 | Intron | NP_001167637.1 | ||||
NM_004694.4 | Intron | NP_004685.2 | ||||
XM_005257789.3 | Intron | XP_005257846.2 | ||||
XM_011525461.2 | Intron | XP_011523763.1 | ||||
XM_017025291.1 | Intron | XP_016880780.1 | ||||
XM_017025292.1 | Intron | XP_016880781.1 |