Product Details

SNP ID
rs8092621
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:61814683 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATATCAACAAGAGGAAACAGGAATT[A/C]TAACTGGCTTAACTCTTGTGGAAGA
Phenotype
MIM: 616512
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
RNF152 PubMed Links

Gene Details

Gene
RNF152
Gene Name
ring finger protein 152
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173557.2 2394 Intron NP_775828.1
XM_005266650.3 2394 UTR 3 XP_005266707.1
XM_005266652.3 2394 UTR 3 XP_005266709.1
XM_011525878.2 2394 UTR 3 XP_011524180.1
XM_011525879.2 2394 UTR 3 XP_011524181.1
XM_017025612.1 2394 UTR 3 XP_016881101.1
XM_017025613.1 2394 UTR 3 XP_016881102.1

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