Product Details

SNP ID
rs137963759
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:50426967 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGTTCCCAGTAGCTTCACTGCCT[C/T]TGCAGCAGCACAGTAAGTAAAGCTG
Phenotype
MIM: 610465
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ACSF2 PubMed Links

Gene Details

Gene
ACSF2
Gene Name
acyl-CoA synthetase family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288968.1 295 Missense Mutation TCT,TTT S64F NP_001275897.1
NM_001288969.1 295 Intron NP_001275898.1
NM_001288970.1 295 Intron NP_001275899.1
NM_001288971.1 295 Intron NP_001275900.1
NM_001288972.1 295 Intron NP_001275901.1
NM_025149.5 295 Intron NP_079425.3
XM_006722110.3 295 Intron XP_006722173.1
XM_011525294.1 295 Intron XP_011523596.1

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