Product Details

SNP ID

rs78018668

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:86567907 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAAGGAGCCGCCCCCGGCGGCGT[C/T]CAAGGGCGCCCCGGCCACCCCCCAC

Phenotype

MIM: 602402

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXC2 PubMed Links

Gene Details

Gene

FOXC2

Gene Name

forkhead box C2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005251.2	657	Missense Mutation	TCC,TTC	S191F	NP_005242.1

Gene

FOXC2-AS1

Gene Name

FOXC2 antisense RNA 1

There are no transcripts associated with this gene.

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