Product Details

SNP ID
rs199926847
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:155660179 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGACTCTGGGCCACAGCCGCATT[C/G]ACAGGCTGGATCATGTTACAGCCAC
Phenotype
MIM: 607860
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
YY1AP1 PubMed Links

Gene Details

Gene
YY1AP1
Gene Name
YY1 associated protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198899.1 2337 Silent Mutation GTC,GTG V566V NP_001185828.1
NM_001198900.1 2337 Silent Mutation GTC,GTG V566V NP_001185829.1
NM_001198901.1 2337 Silent Mutation GTC,GTG V577V NP_001185830.1
NM_001198902.1 2337 Silent Mutation GTC,GTG V577V NP_001185831.1
NM_001198903.1 2337 Silent Mutation GTC,GTG V715V NP_001185832.1
NM_001198904.1 2337 Silent Mutation GTC,GTG V695V NP_001185833.1
NM_001198905.1 2337 Silent Mutation GTC,GTG V557V NP_001185834.1
NM_001198906.1 2337 UTR 3 NP_001185835.1
NM_018253.3 2337 Silent Mutation GTC,GTG V566V NP_060723.2
NM_139118.2 2337 Silent Mutation GTC,GTG V623V NP_620829.1
NM_139119.2 2337 Silent Mutation GTC,GTG V577V NP_620830.1
NM_139121.2 2337 Silent Mutation GTC,GTG V511V NP_620832.1

View Full Product Details