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SNP ID

rs150571747

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:97854193 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCGCTTCCCCTTCTACCGCGACAA[C/T]CCCAAAAAGTGGCAGAACAGCATCC

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	939	Silent Mutation	AAC,AAT	N93N	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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