Product Details

SNP ID

rs61753358

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:55623753 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGACTGTGAATTTTGGTATAGTCT[C/T]CATGGCCAGGTCCCAGGGCTGCTGG

Phenotype

MIM: 300949

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXR2 PubMed Links

Gene Details

Gene

FOXR2

Gene Name

forkhead box R2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198451.3	354	Silent Mutation	CTC,CTT	L14L	NP_940853.1

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