Product Details

SNP ID

rs187090652

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:199911654 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCCGCAGCGCAGCAACGAATTGCT[C/T]CTGTTGGCGGCGGCCGGGGAGGGAC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C2orf69 PubMed Links

Gene Details

Gene

C2orf69

Gene Name

chromosome 2 open reading frame 69

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153689.5	399	Silent Mutation	CTC,CTT	L72L	NP_710156.3

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