Product Details

SNP ID
rs199810314
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:127942535 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCATAGACATCATGTTCTAGATT[C/T]GTCTGCAACACACAAAAGGGAGGGT
Phenotype
MIM: 609697
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SAP130 PubMed Links

Gene Details

Gene
SAP130
Gene Name
Sin3A associated protein 130
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145928.1 2985 Silent Mutation ACA,ACG T994T NP_001139400.1
NM_024545.3 2985 Silent Mutation ACA,ACG T959T NP_078821.2
XM_005263767.3 2985 Silent Mutation ACA,ACG T993T XP_005263824.1
XM_005263768.3 2985 Silent Mutation ACA,ACG T968T XP_005263825.1
XM_005263769.3 2985 Silent Mutation ACA,ACG T968T XP_005263826.1
XM_005263770.3 2985 Silent Mutation ACA,ACG T967T XP_005263827.1
XM_006712748.3 2985 Silent Mutation ACA,ACG T993T XP_006712811.1
XM_006712749.3 2985 Silent Mutation ACA,ACG T958T XP_006712812.1
XM_017004903.1 2985 Silent Mutation ACA,ACG T967T XP_016860392.1
XM_017004904.1 2985 Silent Mutation ACA,ACG T933T XP_016860393.1
XM_017004905.1 2985 Silent Mutation ACA,ACG T932T XP_016860394.1

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