Product Details

SNP ID
rs122458138
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:109661643 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTAACTTCACTAGATCTTTCTTAC[G/T]ATCTGTTAAGTCATAAAGAATGTTA
Phenotype
MIM: 300157
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ACSL4 PubMed Links

Gene Details

Gene
ACSL4
Gene Name
acyl-CoA synthetase long-chain family member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318509.1 2075 Missense Mutation AGT,CGT S570R NP_001305438.1
NM_001318510.1 2075 Missense Mutation AGT,CGT S529R NP_001305439.1
NM_004458.2 2075 Missense Mutation AGT,CGT S529R NP_004449.1
NM_022977.2 2075 Missense Mutation AGT,CGT S570R NP_075266.1
XM_005262109.2 2075 Missense Mutation AGT,CGT S570R XP_005262166.1
XM_006724635.2 2075 Missense Mutation AGT,CGT S529R XP_006724698.1
XM_011530888.2 2075 Missense Mutation AGT,CGT S570R XP_011529190.1
XM_011530889.2 2075 Missense Mutation AGT,CGT S570R XP_011529191.1

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