Product Details

SNP ID
rs59690640
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:93592296 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGCATCAATTTTTTCCCAGATCT[A/G]TATATTAGCAAATTCTGCCTTTGAT
Phenotype
MIM: 132890
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NR2F1 PubMed Links

Gene Details

Gene
NR2F1
Gene Name
nuclear receptor subfamily 2 group F member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005654.5 Intron NP_005645.1
XM_017009797.1 Intron XP_016865286.1

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