Product Details

SNP ID
rs77663197
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:109278487 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGTCAGTAATTAGCAAGGAGAG[A/G]AAAAGAAGCATAAAAACAGCTGCAG
Phenotype
MIM: 609429
Polymorphism
A/G, 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 3032 UTR 3 NP_998761.2
XM_011537922.2 3032 UTR 3 XP_011536224.1
XM_011537923.2 3032 Intron XP_011536225.1
XM_017018818.1 3032 UTR 3 XP_016874307.1
XM_017018819.1 3032 Intron XP_016874308.1

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