Product Details

SNP ID
rs7583955
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:230168572 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCCTGTGAAGCCTGCATGTGCCCC[A/C]AAACCCCCAAATCAAAACAAACCCC
Phenotype
MIM: 604457
Polymorphism
A/C, Transversion 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 2757 Intron NP_001171944.1
NM_004509.3 2757 Intron NP_004500.3
NM_004510.3 2757 Intron NP_004501.3
NM_080424.2 2757 Intron NP_536349.2
XM_005246525.3 2757 UTR 3 XP_005246582.1
XM_006712487.3 2757 Intron XP_006712550.1
XM_006712489.3 2757 UTR 3 XP_006712552.1
XM_011511088.2 2757 UTR 3 XP_011509390.1
XM_011511089.2 2757 UTR 3 XP_011509391.1
XM_011511090.2 2757 UTR 3 XP_011509392.1
XM_011511091.2 2757 UTR 3 XP_011509393.1
XM_011511092.2 2757 UTR 3 XP_011509394.1
XM_017003968.1 2757 UTR 3 XP_016859457.1
XM_017003969.1 2757 Intron XP_016859458.1
XM_017003970.1 2757 Intron XP_016859459.1

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