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GTTAACAATTCTTTACCTACCTATG[C/T]TTATGCACTCCCAAAGTGCAGGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614451 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ELOVL7 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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ELOVL7 - ELOVL fatty acid elongase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001104558.1 | Intron | NP_001098028.1 | ||||
NM_001297617.1 | Intron | NP_001284546.1 | ||||
NM_001297618.1 | Intron | NP_001284547.1 | ||||
NM_024930.2 | Intron | NP_079206.2 | ||||
XM_005248606.4 | Intron | XP_005248663.1 | ||||
XM_005248607.3 | Intron | XP_005248664.1 | ||||
XM_006714695.3 | Intron | XP_006714758.1 | ||||
XM_011543651.2 | Intron | XP_011541953.1 | ||||
XM_017009885.1 | Intron | XP_016865374.1 | ||||
XM_017009886.1 | Intron | XP_016865375.1 | ||||
XM_017009887.1 | Intron | XP_016865376.1 | ||||
XM_017009888.1 | Intron | XP_016865377.1 | ||||
XM_017009889.1 | Intron | XP_016865378.1 |