Product Details

SNP ID
rs1060759
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:230165695 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATTGCCTTAAGTATGTGACACATT[A/G]CAGATATTTTATTTTTGACTTTGAC
Phenotype
MIM: 604457
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SP110 PubMed Links

Gene Details

Gene
SP110
Gene Name
SP110 nuclear body protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001185015.1 5634 Intron NP_001171944.1
NM_004509.3 5634 Intron NP_004500.3
NM_004510.3 5634 Intron NP_004501.3
NM_080424.2 5634 Intron NP_536349.2
XM_005246525.3 5634 UTR 3 XP_005246582.1
XM_006712487.3 5634 Intron XP_006712550.1
XM_006712489.3 5634 UTR 3 XP_006712552.1
XM_011511088.2 5634 UTR 3 XP_011509390.1
XM_011511089.2 5634 UTR 3 XP_011509391.1
XM_011511090.2 5634 UTR 3 XP_011509392.1
XM_011511091.2 5634 UTR 3 XP_011509393.1
XM_011511092.2 5634 UTR 3 XP_011509394.1
XM_017003968.1 5634 UTR 3 XP_016859457.1
XM_017003969.1 5634 Intron XP_016859458.1
XM_017003970.1 5634 Intron XP_016859459.1

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