Product Details

SNP ID
rs202149691
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:109281432 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCAGAGCGAAGTCCATGATGCT[C/T]GGGTCGAGGGCATCCACCTCAGTGT
Phenotype
MIM: 609429
Polymorphism
C/T, Transition 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 1563 Silent Mutation CCA,CCG P423P NP_998761.2
XM_011537922.2 1563 Silent Mutation CCA,CCG P424P XP_011536224.1
XM_011537923.2 1563 Intron XP_011536225.1
XM_017018818.1 1563 Silent Mutation CCA,CCG P380P XP_016874307.1
XM_017018819.1 1563 Intron XP_016874308.1

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