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AGCTCTTCTGCGTGAAGCGCTTGGC[A/G]CAGACGGCGCACTGGAAGGCGCGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603314 | ||||||||||||||||||||
Literature Links: |
SLC27A5 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 |
SLC27A5 - solute carrier family 27 member 5 | ||||||
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There are no transcripts associated with this gene. |
ZBTB45 - zinc finger and BTB domain containing 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316978.1 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_001303907.1 | |
NM_001316979.1 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_001303908.1 | |
NM_001316980.1 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_001303909.1 | |
NM_001316981.1 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_001303910.1 | |
NM_001316982.1 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_001303911.1 | |
NM_032792.3 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | NP_116181.1 | |
XM_006723445.3 | 1703 | Silent Mutation | TGC,TGT | C,C 464 | XP_006723508.1 |