Product Details

SNP ID
rs143881857
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32159112 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATGCTGGTGCTGTGGCTGCCACA[A/G]TCTCAGGAATCTCACACTCATGGCA
Phenotype
Polymorphism
A/G, 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_001010859.1 647 Missense Mutation ACT,ATT T35I NP_001010859.1
XM_011529922.2 647 Intron XP_011528224.1
XM_017028629.1 647 Intron XP_016884118.1
XM_017028630.1 647 Missense Mutation ACT,ATT T49I XP_016884119.1
XM_017028631.1 647 Missense Mutation ACT,ATT T49I XP_016884120.1
XM_017028632.1 647 Intron XP_016884121.1

View Full Product Details