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GGGCCTCCTGGGGACAGCAAGACTG[C/T]CTGGGGAGCGGGAAGCAGCTCCCCC
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1934 | Missense Mutation | ACA,GCA | T,A 455 | NP_699188.1 | |
XM_005256488.3 | 1934 | Missense Mutation | ACA,GCA | T,A 550 | XP_005256545.2 | |
XM_017024281.1 | 1934 | Intron | XP_016879770.1 | |||
XM_017024282.1 | 1934 | Missense Mutation | ACA,GCA | T,A 294 | XP_016879771.1 |
SLC16A13 - solute carrier family 16 member 13 | ||||||
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There are no transcripts associated with this gene. |