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ACTTCCGGGAGACTCGGAAACCTGC[C/T]GCCCGCAAGGCATAGTAAGAGTACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611546 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ELOVL6 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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ELOVL6 - ELOVL fatty acid elongase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130721.1 | 687 | Silent Mutation | GCA,GCG | A,A 185 | NP_001124193.1 | |
NM_024090.2 | 687 | Silent Mutation | GCA,GCG | A,A 185 | NP_076995.1 | |
XM_011532233.2 | 687 | Silent Mutation | GCA,GCG | A,A 185 | XP_011530535.1 | |
XM_011532234.2 | 687 | Silent Mutation | GCA,GCG | A,A 185 | XP_011530536.1 | |
XM_011532235.2 | 687 | Silent Mutation | GCA,GCG | A,A 101 | XP_011530537.1 |