Product Details

SNP ID
rs28420234
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:61810065 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATGGCTTTCCAATAAAATGTATA[C/T]AGTAGAACCTACCTCTTCATATATT
Phenotype
MIM: 616512
Polymorphism
C/T, Transition 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 7012 Intron NP_775828.1
XM_005266650.3 7012 UTR 3 XP_005266707.1
XM_005266652.3 7012 UTR 3 XP_005266709.1
XM_011525878.2 7012 UTR 3 XP_011524180.1
XM_011525879.2 7012 UTR 3 XP_011524181.1
XM_017025612.1 7012 UTR 3 XP_016881101.1
XM_017025613.1 7012 UTR 3 XP_016881102.1

View Full Product Details