Product Details

SNP ID
rs9963722
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:61809236 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCTCTCCCTCTACTTAATAGTTGC[A/G]TTGTCCCTCAACCCAGAAAATCCTA
Phenotype
MIM: 616512
Polymorphism
A/G, 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 7841 Intron NP_775828.1
XM_005266650.3 7841 UTR 3 XP_005266707.1
XM_005266652.3 7841 UTR 3 XP_005266709.1
XM_011525878.2 7841 UTR 3 XP_011524180.1
XM_011525879.2 7841 UTR 3 XP_011524181.1
XM_017025612.1 7841 UTR 3 XP_016881101.1
XM_017025613.1 7841 UTR 3 XP_016881102.1

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