Product Details

SNP ID
rs2219333
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:60753292 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACTCTACTGACTAATAGTTTTGAT[C/T]CTCTGACAAGAAAATGTAAAAATAA
Phenotype
MIM: 614451
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ELOVL7 PubMed Links

Gene Details

Gene
ELOVL7
Gene Name
ELOVL fatty acid elongase 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001104558.1 2745 UTR 3 NP_001098028.1
NM_001297617.1 2745 UTR 3 NP_001284546.1
NM_001297618.1 2745 UTR 3 NP_001284547.1
NM_024930.2 2745 UTR 3 NP_079206.2
XM_005248606.4 2745 UTR 3 XP_005248663.1
XM_005248607.3 2745 UTR 3 XP_005248664.1
XM_006714695.3 2745 UTR 3 XP_006714758.1
XM_011543651.2 2745 UTR 3 XP_011541953.1
XM_017009885.1 2745 UTR 3 XP_016865374.1
XM_017009886.1 2745 UTR 3 XP_016865375.1
XM_017009887.1 2745 UTR 3 XP_016865376.1
XM_017009888.1 2745 Intron XP_016865377.1
XM_017009889.1 2745 Intron XP_016865378.1

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