Product Details

SNP ID
rs201464163
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:75381702 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCTGGCCTTGGCTCTGAATAAACA[C/T]AAGCTGCAAATAAGAAACCTAAGCG
Phenotype
MIM: 607776
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SIN3A PubMed Links

Gene Details

Gene
SIN3A
Gene Name
SIN3 transcription regulator family member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145357.1 3381 Missense Mutation ATG,GTG M1067V NP_001138829.1
NM_001145358.1 3381 Missense Mutation ATG,GTG M1067V NP_001138830.1
NM_015477.2 3381 Missense Mutation ATG,GTG M1067V NP_056292.1
XM_006720465.3 3381 Missense Mutation ATG,GTG M1067V XP_006720528.1
XM_006720466.3 3381 Missense Mutation ATG,GTG M1067V XP_006720529.1
XM_006720467.3 3381 Missense Mutation ATG,GTG M1067V XP_006720530.1

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