Product Details

SNP ID

rs199854559

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:106612085 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGTACGCAGTTATCCAACAATGT[C/G]TGGTGAGTCAGGACAGCCTGAGGCT

Phenotype

Polymorphism

C/G, 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	156	Missense Mutation	TCT,TGT	S2C	NP_001171711.1
NM_018015.5	156	Missense Mutation	TCT,TGT	S2C	NP_060485.4

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