Product Details

SNP ID

rs148686737

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:106612589 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTCTTTAGAAACTCCCTTCAGAA[A/G]TAGAGCGCACCAGGAGAAACCAGAG

Phenotype

Polymorphism

A/G, Transition 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	660	Missense Mutation	AAT,AGT	N170S	NP_001171711.1
NM_018015.5	660	Missense Mutation	AAT,AGT	N170S	NP_060485.4

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