Product Details

SNP ID
rs142916210
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:45151862 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCCTGGAGAAGTCGAGGCAGCAA[C/T]TTCTGACACACCAGCACCAGGCTCT
Phenotype
MIM: 300959
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CXorf36 PubMed Links

Gene Details

Gene
CXorf36
Gene Name
chromosome X open reading frame 36
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024689.2 968 Intron NP_078965.2
NM_176819.3 968 Silent Mutation NP_789789.2
XM_005272670.1 968 Missense Mutation XP_005272727.1
XM_006724559.1 968 Missense Mutation XP_006724622.1

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