Product Details

SNP ID

rs140310025

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:86578845 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCCCGCGGCTGCTCTAGCTGCCT[C/T]GGGCCGGGCCGAGACCCCGCAGAAG

Phenotype

MIM: 602402 MIM: 603252

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXC2 PubMed Links

Gene Details

Gene

FOXC2

Gene Name

forkhead box C2

There are no transcripts associated with this gene.

Gene

FOXL1

Gene Name

forkhead box L1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005250.2	337	Missense Mutation	TCG,TTG	S41L	NP_005241.1

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