Product Details

SNP ID
rs201956712
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:29058921 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCAGCTCCAGGCTGTACCTCTTGG[C/G]GGTCCCTGAAGGATTCCACAGCATT
Phenotype
MIM: 612062
Polymorphism
C/G, 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_015370.1 616 Missense Mutation CCC,GCC P232A NP_056185.1
XM_005261491.3 616 Missense Mutation CCC,GCC P128A XP_005261548.1
XM_011530096.2 616 Missense Mutation CCC,GCC P191A XP_011528398.1
XM_017028741.1 616 Missense Mutation CCC,GCC P191A XP_016884230.1
Gene
ZNRF3
Gene Name
zinc and ring finger 3
There are no transcripts associated with this gene.

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