Product Details

SNP ID
rs140092102
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:43037713 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTACCGGAAGGTAGAGAAGCTCTGG[A/G]TGGCAGTGCAGGAGGCATAGGGCAC
Phenotype
MIM: 609577 MIM: 613475
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CUL7 PubMed Links

Gene Details

Gene
CUL7
Gene Name
cullin 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001168370.1 5448 Missense Mutation ACC,ATC T1775I NP_001161842.1
NM_014780.4 5448 Missense Mutation ACC,ATC T1691I NP_055595.2
XM_005249503.2 5448 Missense Mutation ACC,ATC T1743I XP_005249560.1
XM_006715285.1 5448 Missense Mutation ACC,ATC T1727I XP_006715348.1
XM_011515019.2 5448 Missense Mutation ACC,ATC T1779I XP_011513321.1
XM_011515020.2 5448 Missense Mutation ACC,ATC T1747I XP_011513322.1
XM_011515021.1 5448 Missense Mutation ACC,ATC T982I XP_011513323.1
XM_017011533.1 5448 Missense Mutation ACC,ATC T1788I XP_016867022.1
XM_017011534.1 5448 Missense Mutation ACC,ATC T1784I XP_016867023.1
XM_017011535.1 5448 Missense Mutation ACC,ATC T1756I XP_016867024.1
XM_017011536.1 5448 Missense Mutation ACC,ATC T1736I XP_016867025.1
XM_017011537.1 5448 Missense Mutation ACC,ATC T1723I XP_016867026.1
XM_017011538.1 5448 Missense Mutation ACC,ATC T1704I XP_016867027.1
XM_017011539.1 5448 Missense Mutation ACC,ATC T1695I XP_016867028.1
XM_017011540.1 5448 Intron XP_016867029.1
Gene
RRP36
Gene Name
ribosomal RNA processing 36
There are no transcripts associated with this gene.

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