Product Details

SNP ID

rs149552852

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:139956001 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCACTATAATATTTCATCGTATC[A/T]CTGTCATTCACATGATCACCGTATG

Phenotype

Polymorphism

A/T, 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	1003	Missense Mutation	AGA,AGT	R327S	NP_001013421.1

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