Product Details

SNP ID
rs17041278
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:110052192 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACCTGGAGGGGACTGGTGACTTGT[C/T]TTAGATCATTTATCAATCAAAGGAA
Phenotype
MIM: 611546
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ELOVL6 PubMed Links

Gene Details

Gene
ELOVL6
Gene Name
ELOVL fatty acid elongase 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130721.1 Intron NP_001124193.1
NM_024090.2 Intron NP_076995.1
XM_011532233.2 Intron XP_011530535.1
XM_011532234.2 Intron XP_011530536.1
XM_011532235.2 Intron XP_011530537.1

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