Product Details

SNP ID
rs149060377
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:118979088 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACACTCCCCTCCTCTCAGCCACCC[C/G]AGAAGGAGGAAGATGCCAGCTGCTC
Phenotype
MIM: 615755
Polymorphism
C/G, Transversion 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_181721.2 493 Missense Mutation CAG,GAG Q90E NP_859072.1
XM_017017575.1 493 Missense Mutation CAG,GAG Q90E XP_016873064.1
XM_017017576.1 493 Missense Mutation CAG,GAG Q90E XP_016873065.1

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