Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGTGAACCTGCGGCGCGAGCCCCT[A/G]GCCTTCTGCCTGGGCACCTCGGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600691 | ||||||||||||||||||||
Literature Links: |
SLC27A1 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 |
SLC27A1 - solute carrier family 27 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198580.2 | 538 | Silent Mutation | CTA,CTG | L,L 167 | NP_940982.1 | |
XM_011528000.1 | 538 | Silent Mutation | CTA,CTG | L,L 167 | XP_011526302.1 | |
XM_011528001.2 | 538 | Silent Mutation | CTA,CTG | L,L 167 | XP_011526303.1 | |
XM_011528002.2 | 538 | Silent Mutation | CTA,CTG | L,L 167 | XP_011526304.1 | |
XM_011528003.2 | 538 | Silent Mutation | CTA,CTG | L,L 167 | XP_011526305.1 | |
XM_017026781.1 | 538 | Silent Mutation | CTA,CTG | L,L 167 | XP_016882270.1 |