Product Details

SNP ID
rs141536949
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:106612266 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGACTCACCTCGCCAGTGTGTCAC[C/T]CCCTCGGAGGTGGTGCCTGTAACTG
Phenotype
Polymorphism
C/T, 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_001184782.1 337 Silent Mutation ACC,ACT T62T NP_001171711.1
NM_018015.5 337 Silent Mutation ACC,ACT T62T NP_060485.4

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