Product Details

SNP ID
rs7292708
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:29073142 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCACTGACGGCCCATGGCGCCGCC[A/C]GCCGCCCGCCTCGCCCTGCTCTCCG
Phenotype
MIM: 609898
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
C22orf31 PubMed Links

Gene Details

Gene
C22orf31
Gene Name
chromosome 22 open reading frame 31
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015370.1 65 Intron NP_056185.1
XM_005261491.3 65 Intron XP_005261548.1
XM_011530096.2 65 Intron XP_011528398.1
XM_017028741.1 65 Intron XP_016884230.1
Gene
KREMEN1
Gene Name
kringle containing transmembrane protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039570.2 65 Silent Mutation CCA,CCC P4P NP_001034659.2
NM_032045.4 65 Silent Mutation CCA,CCC P4P NP_114434.3
XM_011530429.2 65 Silent Mutation CCA,CCC P4P XP_011528731.1
XM_011530430.2 65 Silent Mutation CCA,CCC P4P XP_011528732.1
XM_011530431.2 65 Intron XP_011528733.1
XM_011530432.2 65 Intron XP_011528734.1
XM_017028989.1 65 Silent Mutation CCA,CCC P4P XP_016884478.1

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