Product Details

SNP ID

rs149817919

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:30559535 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCAGTTGACATCAATTGCAATAGG[C/T]GGCTAAAGACTATATCTCTGGCTTT

Phenotype

Polymorphism

C/T, Transition 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	1216	Missense Mutation	CAC,CGC	H274R	NP_079435.1

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