Product Details

SNP ID
rs2608743
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:16830599 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGACTCAGATTCTTGGAAGTCACAT[C/G]CTTACCATACTGCTGCCCCCTCTTA
Phenotype
MIM: 607777
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SIN3B PubMed Links

Gene Details

Gene
SIN3B
Gene Name
SIN3 transcription regulator family member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297595.1 Intron NP_001284524.1
NM_001297597.1 Intron NP_001284526.1
NM_015260.3 Intron NP_056075.1
XM_006722704.1 Intron XP_006722767.1

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