Product Details

SNP ID

rs3191540

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:89162724 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCCTCTTCCGTGTCGCTGGGGCTC[T/G]CGTGGCTCCGGAAGCTCCCCTCGCT

Phenotype

MIM: 602628

Polymorphism

T/G, Transversion 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	1351	Intron			NP_001078940.1
NM_005197.3	1351	Missense Mutation	GAG,GCG	E366A	NP_005188.2

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