Product Details

SNP ID
rs6545031
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:48331121 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTACCCAAAGAGGTAATAAGGAAAG[A/C]TATTCAGTGACTGGCTCAAGGGTAC
Phenotype
MIM: 143089
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
FOXN2 PubMed Links

Gene Details

Gene
FOXN2
Gene Name
forkhead box N2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002158.3 Intron NP_002149.2
XM_005264282.2 Intron XP_005264339.1
XM_005264283.2 Intron XP_005264340.1
XM_006712001.3 Intron XP_006712064.1
XM_006712002.3 Intron XP_006712065.1
XM_011532808.2 Intron XP_011531110.1
XM_017003956.1 Intron XP_016859445.1
XM_017003957.1 Intron XP_016859446.1
XM_017003958.1 Intron XP_016859447.1
XM_017003959.1 Intron XP_016859448.1

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