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GTCAAGGAAGAGTCCAGAAACCGCC[A/G]TCATTGGCTTCATGAAAACCGAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604457 | ||||||||||||||||||||
Literature Links: |
SP110 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SP110 - SP110 nuclear body protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185015.1 | 2181 | Intron | NP_001171944.1 | |||
NM_004509.3 | 2181 | Silent Mutation | GAC,GAT | D,D 682 | NP_004500.3 | |
NM_004510.3 | 2181 | Intron | NP_004501.3 | |||
NM_080424.2 | 2181 | Silent Mutation | GAC,GAT | D,D 706 | NP_536349.2 | |
XM_005246525.3 | 2181 | Silent Mutation | GAC,GAT | D,D 712 | XP_005246582.1 | |
XM_006712487.3 | 2181 | Silent Mutation | GAC,GAT | D,D 688 | XP_006712550.1 | |
XM_006712489.3 | 2181 | Silent Mutation | GAC,GAT | D,D 641 | XP_006712552.1 | |
XM_011511088.2 | 2181 | Silent Mutation | GAC,GAT | D,D 738 | XP_011509390.1 | |
XM_011511089.2 | 2181 | Silent Mutation | GAC,GAT | D,D 732 | XP_011509391.1 | |
XM_011511090.2 | 2181 | Silent Mutation | GAC,GAT | D,D 688 | XP_011509392.1 | |
XM_011511091.2 | 2181 | Silent Mutation | GAC,GAT | D,D 665 | XP_011509393.1 | |
XM_011511092.2 | 2181 | Silent Mutation | GAC,GAT | D,D 529 | XP_011509394.1 | |
XM_017003968.1 | 2181 | Silent Mutation | GAC,GAT | D,D 738 | XP_016859457.1 | |
XM_017003969.1 | 2181 | Intron | XP_016859458.1 | |||
XM_017003970.1 | 2181 | Intron | XP_016859459.1 |