Product Details

SNP ID

rs200132999

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:97854216 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCCCAAAAAGTGGCAGAACAGCA[C/T]CCGCCACAACCTCACACTCAACGAC

Phenotype

MIM: 602617

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXE1 PubMed Links

Gene Details

Gene

FOXE1

Gene Name

forkhead box E1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004473.3	962	Missense Mutation	ACC,ATC	T101I	NP_004464.2

Gene

PTCSC2

Gene Name

papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding)

There are no transcripts associated with this gene.

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