Product Details

SNP ID
rs6737596
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:230422621 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATGCCCCTATCTTCCAAAATGTTT[C/G]ATTATCTCTTATTTGATGCCCTTTT
Phenotype
MIM: 604585
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SP100 PubMed Links

Gene Details

Gene
SP100
Gene Name
SP100 nuclear antigen
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080391.1 Intron NP_001073860.1
NM_001206701.1 Intron NP_001193630.1
NM_001206702.1 Intron NP_001193631.1
NM_001206703.1 Intron NP_001193632.1
NM_001206704.1 Intron NP_001193633.1
NM_003113.3 Intron NP_003104.2

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