Product Details

SNP ID
rs191329509
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:156325971 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAATCTTGTTTTGCAGTTCTTCCA[C/G]TCTCTTGGGTTCCTTGAGCCCGTGT
Phenotype
MIM: 601828
Polymorphism
C/G, 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 3701 Missense Mutation CTG,GTG L524V NP_006177.1
XM_005246621.3 3701 Missense Mutation CTG,GTG L535V XP_005246678.1
XM_005246622.3 3701 Missense Mutation CTG,GTG L461V XP_005246679.1
XM_006712553.3 3701 Missense Mutation CTG,GTG L510V XP_006712616.1
XM_011511246.1 3701 Missense Mutation ACT,AGT T500S XP_011509548.1
XM_017004219.1 3701 Missense Mutation CTG,GTG L524V XP_016859708.1
XM_017004220.1 3701 Missense Mutation CTG,GTG L499V XP_016859709.1

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