Product Details

SNP ID

rs151247663

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:106622692 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTTCTCATCTTGAAATGACCTGG[A/T]CTAACAGAAGAAATTTTCCTGCATT

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CXorf57 PubMed Links

Gene Details

Gene

CXorf57

Gene Name

chromosome X open reading frame 57

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184782.1	836	Missense Mutation	ACT,TCT	T229S	NP_001171711.1
NM_018015.5	836	Missense Mutation	ACT,TCT	T229S	NP_060485.4

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