Product Details

SNP ID
rs201710177
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32159215 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCAGCAAGTCAGTTTGCTCCCCA[C/T]TGGGCACCTAAACACACAAAAAAGT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C22orf42 PubMed Links

Gene Details

Gene
C22orf42
Gene Name
chromosome 22 open reading frame 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010859.1 544 Missense Mutation ATG,GTG M1V NP_001010859.1
XM_011529922.2 544 Intron XP_011528224.1
XM_017028629.1 544 Intron XP_016884118.1
XM_017028630.1 544 Missense Mutation ATG,GTG M15V XP_016884119.1
XM_017028631.1 544 Missense Mutation ATG,GTG M15V XP_016884120.1
XM_017028632.1 544 Intron XP_016884121.1

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