Product Details

SNP ID
rs9966069
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:61809202 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATAGACCCAGTGCTTCATGTCTCCC[C/T]TTCCCTCTCCCTCTCCCTCTACTTA
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 7875 Intron NP_775828.1
XM_005266650.3 7875 UTR 3 XP_005266707.1
XM_005266652.3 7875 UTR 3 XP_005266709.1
XM_011525878.2 7875 UTR 3 XP_011524180.1
XM_011525879.2 7875 UTR 3 XP_011524181.1
XM_017025612.1 7875 UTR 3 XP_016881101.1
XM_017025613.1 7875 UTR 3 XP_016881102.1

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