Product Details

SNP ID

rs138947666

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:139955925 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCATTTAGGGTTACTTCAGAGGTGA[C/G]TTGATTGTACCCTCTGTCACACGTA

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	1079	Missense Mutation	CTC,GTC	L353V	NP_001013421.1

View Full Product Details