Product Details

SNP ID
rs200708160
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:109279780 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGGAGTACGCTGTGTAGAGACCC[G/T]TCACCTGCAAGTCTGGGAAGGACTG
Phenotype
MIM: 609429
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FOXN4 PubMed Links

Gene Details

Gene
FOXN4
Gene Name
forkhead box N4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_213596.2 1739 Missense Mutation NP_998761.2
XM_011537922.2 1739 Missense Mutation XP_011536224.1
XM_011537923.2 1739 Intron XP_011536225.1
XM_017018818.1 1739 Missense Mutation XP_016874307.1
XM_017018819.1 1739 Intron XP_016874308.1

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