Product Details

SNP ID
rs202015594
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:6211742 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGTTGAAGCCCCAGGGGAGCCCC[C/G]ACTTAGGCCAAGTCCTGCTCCGTCT
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
C11orf42 PubMed Links

Gene Details

Gene
C11orf42
Gene Name
chromosome 11 open reading frame 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173525.2 3020 Intron NP_775796.2
XM_011519926.2 3020 Intron XP_011518228.1
XM_011519927.2 3020 Intron XP_011518229.1
Gene
FAM160A2
Gene Name
family with sequence similarity 160 member A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098794.1 3020 Missense Mutation CGG,GGG R895G NP_001092264.1
NM_032127.3 3020 Missense Mutation CGG,GGG R909G NP_115503.2
XM_006718343.2 3020 Missense Mutation CGG,GGG R909G XP_006718406.1
XM_011520397.2 3020 Missense Mutation CGG,GGG R909G XP_011518699.1
XM_011520398.2 3020 Intron XP_011518700.1
XM_011520399.2 3020 Intron XP_011518701.1

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