Product Details

SNP ID
rs148151608
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:45151851 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGGGGAACCTCCCCTGGAGAAGT[C/T]GAGGCAGCAACTTCTGACACACCAG
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_024689.2 979 Intron NP_078965.2
NM_176819.3 979 Missense Mutation CAA,CGA Q368R NP_789789.2
XM_005272670.1 979 Missense Mutation CAA,CGA Q310R XP_005272727.1
XM_006724559.1 979 Missense Mutation CAA,CGA Q284R XP_006724622.1

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