Product Details

SNP ID
rs141906487
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:127945510 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGACTTTCCAGCCTTGAGCACGACA[C/G]GATACTCCTTTCTGATTAGCTATTT
Phenotype
MIM: 609697
Polymorphism
C/G, Transversion 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 2928 Silent Mutation TCC,TCG S975S NP_001139400.1
NM_024545.3 2928 Silent Mutation TCC,TCG S940S NP_078821.2
XM_005263767.3 2928 Silent Mutation TCC,TCG S974S XP_005263824.1
XM_005263768.3 2928 Silent Mutation TCC,TCG S949S XP_005263825.1
XM_005263769.3 2928 Silent Mutation TCC,TCG S949S XP_005263826.1
XM_005263770.3 2928 Silent Mutation TCC,TCG S948S XP_005263827.1
XM_006712748.3 2928 Silent Mutation TCC,TCG S974S XP_006712811.1
XM_006712749.3 2928 Silent Mutation TCC,TCG S939S XP_006712812.1
XM_017004903.1 2928 Silent Mutation TCC,TCG S948S XP_016860392.1
XM_017004904.1 2928 Silent Mutation TCC,TCG S914S XP_016860393.1
XM_017004905.1 2928 Silent Mutation TCC,TCG S913S XP_016860394.1

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