Product Details

SNP ID
rs141702033
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:28513785 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCATGACCCAGAGCCCACTGTGA[A/G]TGCTTGGATTTGGCTCCTTTGGGGC
Phenotype
MIM: 600838
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FOXN1 PubMed Links

Gene Details

Gene
FOXN1
Gene Name
forkhead box N1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003593.2 Intron NP_003584.2
XM_005258046.3 Intron XP_005258103.1
XM_011525358.1 Intron XP_011523660.1
XM_011525359.1 Intron XP_011523661.1
XM_011525362.1 Intron XP_011523664.1
XM_011525367.1 Intron XP_011523669.1
XM_011525368.2 Intron XP_011523670.1
XM_011525369.2 Intron XP_011523671.1
XM_011525370.2 Intron XP_011523672.1
XM_017025228.1 Intron XP_016880717.1
XM_017025229.1 Intron XP_016880718.1
XM_017025230.1 Intron XP_016880719.1
XM_017025231.1 Intron XP_016880720.1

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