Product Details

SNP ID
rs201429282
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32150450 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCATGAAGTCTTCAAGACAGACAG[A/T]TAGGCTTTCACTGAGATCTTCGACC
Phenotype
Polymorphism
A/T, Transversion 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_001010859.1 973 Missense Mutation ACT,TCT T175S NP_001010859.1
XM_011529922.2 973 Intron XP_011528224.1
XM_017028629.1 973 Intron XP_016884118.1
XM_017028630.1 973 Missense Mutation ACT,TCT T158S XP_016884119.1
XM_017028631.1 973 UTR 3 XP_016884120.1
XM_017028632.1 973 Intron XP_016884121.1

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