Product Details

SNP ID
rs143117752
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:118979121 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAGATGCCAGCTGCTCAGAGGCC[A/G]CAGGGGTGGAATCACTGTCCCAGTC
Phenotype
MIM: 615755
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FOXR1 PubMed Links

Gene Details

Gene
FOXR1
Gene Name
forkhead box R1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181721.2 526 Missense Mutation ACA,GCA T101A NP_859072.1
XM_017017575.1 526 Missense Mutation ACA,GCA T101A XP_016873064.1
XM_017017576.1 526 Missense Mutation ACA,GCA T101A XP_016873065.1

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