Product Details

SNP ID
rs4911163
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:34882891 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGATGTGACTAAAGGGAAAATCTT[C/T]ATTGAGTGGATGAAAGGAGCAACTA
Phenotype
MIM: 605832
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ACSS2 PubMed Links

Gene Details

Gene
ACSS2
Gene Name
acyl-CoA synthetase short-chain family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001076552.2 350 Silent Mutation TTC,TTT F92F NP_001070020.2
NM_001242393.1 350 UTR 5 NP_001229322.1
NM_018677.3 350 Silent Mutation TTC,TTT F92F NP_061147.1
XM_005260455.1 350 Silent Mutation TTC,TTT F92F XP_005260512.1
XM_005260456.1 350 Silent Mutation TTC,TTT F92F XP_005260513.1
XM_006723826.1 350 UTR 5 XP_006723889.1
XM_011528905.1 350 Silent Mutation TTC,TTT F92F XP_011527207.1
XM_011528906.1 350 Silent Mutation TTC,TTT F92F XP_011527208.1
XM_011528907.1 350 Silent Mutation TTC,TTT F92F XP_011527209.1
XM_011528908.1 350 Silent Mutation TTC,TTT F92F XP_011527210.1
XM_011528909.2 350 Silent Mutation TTC,TTT F42F XP_011527211.1
XM_011528911.1 350 Silent Mutation TTC,TTT F42F XP_011527213.1
XM_011528912.2 350 UTR 5 XP_011527214.1

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