Product Details

SNP ID

rs202031875

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:86579468 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGTCCCCTCTGCGCCCCGCCTCC[C/T]GCAGCTCTCCGAAGAGCTCCGACAA

Phenotype

MIM: 603252

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXL1 PubMed Links

Gene Details

Gene

FOXL1

Gene Name

forkhead box L1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005250.2	960	Missense Mutation	CGC,TGC	R249C	NP_005241.1

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