Product Details

SNP ID
rs199982165
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:200913982 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAGCTGGTATTTTATTAGTAGCC[C/T]GAAAATTCCCCTAAAAAAAAAAAAA
Phenotype
MIM: 601182
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ORC2 PubMed Links

Gene Details

Gene
ORC2
Gene Name
origin recognition complex subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006190.4 1810 Missense Mutation AGG,GGG R493G NP_006181.1
XM_006712555.3 1810 Missense Mutation AGG,GGG R493G XP_006712618.1
XM_011511252.2 1810 Missense Mutation AGG,GGG R513G XP_011509554.1
XM_011511253.2 1810 Missense Mutation AGG,GGG R513G XP_011509555.1

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