Product Details

SNP ID
rs202217305
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:6211637 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACTCCTTGAGAAATTCAGGGAAAA[C/T]GACTGCACAGTAGACAGCATTCTTG
Phenotype
Polymorphism
C/T, Transition 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 3125 Intron NP_775796.2
XM_011519926.2 3125 Intron XP_011518228.1
XM_011519927.2 3125 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 3125 Missense Mutation ATT,GTT I930V NP_001092264.1
NM_032127.3 3125 Missense Mutation ATT,GTT I944V NP_115503.2
XM_006718343.2 3125 Missense Mutation ATT,GTT I944V XP_006718406.1
XM_011520397.2 3125 Missense Mutation ATT,GTT I944V XP_011518699.1
XM_011520398.2 3125 Intron XP_011518700.1
XM_011520399.2 3125 Intron XP_011518701.1

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