Product Details

SNP ID
rs1110467
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:19410402 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTGCAGAGGCAGGGAAGAGTGGGG[C/T]GAGAGAAGGGTGGAAGGAAGGTTCA
Phenotype
MIM: 601237
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF112 PubMed Links

Gene Details

Gene
RNF112
Gene Name
ring finger protein 112
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007148.4 3234 Intron NP_009079.2
XM_006721571.3 3234 UTR 5 XP_006721634.1
XM_006721572.3 3234 UTR 5 XP_006721635.1
XM_006721573.3 3234 Intron XP_006721636.1

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