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CAGTCAAGGTATGTAACTTTTAGAG[C/T]CCCAGTTTTCTCATTTTGGAAATAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603654 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC16A7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SLC16A7 - solute carrier family 16 member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270622.1 | Intron | NP_001257551.1 | ||||
NM_001270623.1 | Intron | NP_001257552.1 | ||||
NM_004731.4 | Intron | NP_004722.2 | ||||
XM_005269231.4 | Intron | XP_005269288.1 | ||||
XM_011538989.2 | Intron | XP_011537291.1 | ||||
XM_011538990.2 | Intron | XP_011537292.1 | ||||
XM_011538991.2 | Intron | XP_011537293.1 | ||||
XM_011538992.2 | Intron | XP_011537294.1 | ||||
XM_011538993.2 | Intron | XP_011537295.1 | ||||
XM_011538995.2 | Intron | XP_011537297.1 | ||||
XM_017020224.1 | Intron | XP_016875713.1 | ||||
XM_017020225.1 | Intron | XP_016875714.1 | ||||
XM_017020226.1 | Intron | XP_016875715.1 | ||||
XM_017020227.1 | Intron | XP_016875716.1 |