Product Details

SNP ID

rs182789066

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:139956264 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACCTTTTTGGATTAAAATGTTTGG[C/G]AGGCTTAGCCAATTCCTGTGGACCG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CXorf66 PubMed Links

Gene Details

Gene

CXorf66

Gene Name

chromosome X open reading frame 66

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013403.2	740	Missense Mutation	CCC,GCC	P240A	NP_001013421.1

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