Product Details

SNP ID
rs5998268
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32160075 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAAATATCTGGCAAGCCTGACAGT[A/G]TTCCAACAGTGGTATACTAATTTAA
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_001010859.1 362 Intron NP_001010859.1
XM_011529922.2 362 Intron XP_011528224.1
XM_017028629.1 362 Intron XP_016884118.1
XM_017028630.1 362 UTR 5 XP_016884119.1
XM_017028631.1 362 UTR 5 XP_016884120.1
XM_017028632.1 362 Intron XP_016884121.1

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