Product Details

SNP ID

rs150949392

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:30559994 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCTGTAAGTCATTATAATTCTTG[A/C]AAATACTTTTGCAAGAAGATGGAAC

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CXorf21 PubMed Links

Gene Details

Gene

CXorf21

Gene Name

chromosome X open reading frame 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025159.2	757	Missense Mutation	TGC,TTC	C121F	NP_079435.1

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