Product Details

SNP ID
rs13070538
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:14966042 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGAGCTTAGTAATTTTAAACTGC[A/T]TATAATAACTATATATAATATTTGA
Phenotype
MIM: 601426
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
NR2C2 PubMed Links

Gene Details

Gene
NR2C2
Gene Name
nuclear receptor subfamily 2 group C member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291694.1 Intron NP_001278623.1
NM_003298.4 Intron NP_003289.2
XM_011534058.2 Intron XP_011532360.1
XM_011534059.2 Intron XP_011532361.1
XM_011534061.2 Intron XP_011532363.1
XM_011534063.2 Intron XP_011532365.1
XM_011534064.2 Intron XP_011532366.1
XM_011534065.2 Intron XP_011532367.1
XM_011534066.2 Intron XP_011532368.1
XM_017007118.1 Intron XP_016862607.1
XM_017007119.1 Intron XP_016862608.1
XM_017007120.1 Intron XP_016862609.1

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