Product Details

SNP ID
rs146939582
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:29058998 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGTAACCCTCTGTGGGGAGACCA[C/T]GGATGGTTAGCGTGTCCTCCGACAA
Phenotype
MIM: 612062
Polymorphism
C/T, Transition 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_015370.1 539 Missense Mutation CAT,CGT H206R NP_056185.1
XM_005261491.3 539 Missense Mutation CAT,CGT H102R XP_005261548.1
XM_011530096.2 539 Missense Mutation CAT,CGT H165R XP_011528398.1
XM_017028741.1 539 Missense Mutation CAT,CGT H165R XP_016884230.1
Gene
ZNRF3
Gene Name
zinc and ring finger 3
There are no transcripts associated with this gene.

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