Product Details

SNP ID
rs36124939
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:41349234 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCAAGACTGTCCGTGTGGACCCTG[A/G]CTCACAGGTGAATGGAAATATACAA
Phenotype
MIM: 612818
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NUSAP1 PubMed Links

Gene Details

Gene
NUSAP1
Gene Name
nucleolar and spindle associated protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243142.1 417 Missense Mutation GAC,GGC D100G NP_001230071.1
NM_001243143.1 417 Missense Mutation GAC,GGC D100G NP_001230072.1
NM_001243144.1 417 Missense Mutation GAC,GGC D77G NP_001230073.1
NM_001301136.1 417 Missense Mutation GAC,GGC D100G NP_001288065.1
NM_016359.4 417 Missense Mutation GAC,GGC D100G NP_057443.2
NM_018454.7 417 Missense Mutation GAC,GGC D100G NP_060924.4
XM_005254428.2 417 Missense Mutation GAC,GGC D100G XP_005254485.1
XM_005254430.4 417 Missense Mutation GAC,GGC D100G XP_005254487.1
XM_005254431.2 417 Missense Mutation GAC,GGC D100G XP_005254488.1
XM_006720559.2 417 Missense Mutation GAC,GGC D100G XP_006720622.1
XM_006720560.3 417 Missense Mutation GAC,GGC D100G XP_006720623.1
XM_006720561.2 417 Missense Mutation GAC,GGC D100G XP_006720624.1
XM_006720562.2 417 Missense Mutation GAC,GGC D100G XP_006720625.1
XM_006720563.2 417 Missense Mutation GAC,GGC D100G XP_006720626.1
XM_017022294.1 417 Missense Mutation GAC,GGC D100G XP_016877783.1
XM_017022295.1 417 UTR 5 XP_016877784.1

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