Product Details

SNP ID

rs16940105

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:109281088 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGATGCCTATGGAATGCTTTGGCC[C/T]GGTATACAGCAAATGCTCATTCCCT

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		Intron			NP_998761.2
XM_011537922.2		Intron			XP_011536224.1
XM_011537923.2		Intron			XP_011536225.1
XM_017018818.1		Intron			XP_016874307.1
XM_017018819.1		Intron			XP_016874308.1

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