Product Details

SNP ID
rs61729997
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:156325941 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGAAAGTCACGTGGTCTTTGAGAC[A/C]ATTTACAATCTTGTTTTGCAGTTCT
Phenotype
MIM: 601828
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
NR4A2 PubMed Links

Gene Details

Gene
NR4A2
Gene Name
nuclear receptor subfamily 4 group A member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006186.3 3731 Missense Mutation GGT,TGT G534C NP_006177.1
XM_005246621.3 3731 Missense Mutation GGT,TGT G545C XP_005246678.1
XM_005246622.3 3731 Missense Mutation GGT,TGT G471C XP_005246679.1
XM_006712553.3 3731 Missense Mutation GGT,TGT G520C XP_006712616.1
XM_011511246.1 3731 Missense Mutation TGG,TTG W510L XP_011509548.1
XM_017004219.1 3731 Missense Mutation GGT,TGT G534C XP_016859708.1
XM_017004220.1 3731 Missense Mutation GGT,TGT G509C XP_016859709.1

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