Product Details

SNP ID
rs201451895
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:122854122 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGAAAAAAAGAAAAGTTAGCTTC[C/G]AACTATAGCTTTCAACTGTCATTCT
Phenotype
MIM: 615231
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
RC3H2 PubMed Links

Gene Details

Gene
RC3H2
Gene Name
ring finger and CCCH-type domains 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001100588.1 Intron NP_001094058.1
NM_018835.2 Intron NP_061323.2

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