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AACTCCCCGCGCTCAGCCCATAGGC[C/T]ACAGCCGCGGCCAGCAGGGGACCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615765 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC16A11 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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SLC16A11 - solute carrier family 16 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153357.1 | 1612 | Silent Mutation | GTA,GTG | V,V 347 | NP_699188.1 | |
XM_005256488.3 | 1612 | Silent Mutation | GTA,GTG | V,V 442 | XP_005256545.2 | |
XM_017024281.1 | 1612 | Silent Mutation | GTA,GTG | V,V 442 | XP_016879770.1 | |
XM_017024282.1 | 1612 | Intron | XP_016879771.1 |
SLC16A13 - solute carrier family 16 member 13 | ||||||
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There are no transcripts associated with this gene. |