Product Details

SNP ID

rs199923188

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:89162581 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCGGTGCGTCTCTTTTTGAGGG[A/G]CAGTGTGTCGCTGGGGACCTTCCTG

Phenotype

MIM: 602628

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FOXN3 PubMed Links

Gene Details

Gene

FOXN3

Gene Name

forkhead box N3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085471.1	1494	Intron			NP_001078940.1
NM_005197.3	1494	Missense Mutation	CCC,TCC	P414S	NP_005188.2

View Full Product Details