Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGAGGATGCCCCAGGCCCTGGAGC[A/G]TGCAGATGGCAGCTGGGCCTGGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603879 | ||||||||||||||||||||
Literature Links: |
SLC16A5 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 |
SLC16A5 - solute carrier family 16 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271765.1 | 268 | Missense Mutation | CAT,CGT | H,R 7 | NP_001258694.1 | |
NM_004695.3 | 268 | Missense Mutation | CAT,CGT | H,R 7 | NP_004686.1 | |
XM_005257790.1 | 268 | Missense Mutation | CAT,CGT | H,R 47 | XP_005257847.1 | |
XM_011525462.1 | 268 | Missense Mutation | CAT,CGT | H,R 47 | XP_011523764.1 | |
XM_017025293.1 | 268 | UTR 5 | XP_016880782.1 |