Product Details

SNP ID
rs183794856
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:118979178 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAGCGGTCTCCCCCTCGGAAGCGG[C/T]TTGCCTTTTCCCCCAGCACCTGGGA
Phenotype
MIM: 615755
Polymorphism
C/T, 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_181721.2 583 Missense Mutation CTT,TTT L120F NP_859072.1
XM_017017575.1 583 Missense Mutation CTT,TTT L120F XP_016873064.1
XM_017017576.1 583 Missense Mutation CTT,TTT L120F XP_016873065.1

View Full Product Details