Product Details

SNP ID
rs11724371
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:1058337 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCACTACCTGAGAGGCTTTCCCA[C/T]GCTCCTCTGACTCGTTGTCAGGCCG
Phenotype
MIM: 612041
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF212 PubMed Links

Gene Details

Gene
RNF212
Gene Name
ring finger protein 212
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001131034.3 471 Intron NP_001124506.1
NM_001193318.2 471 Intron NP_001180247.1
NM_194439.4 471 Intron NP_919420.1
XM_005272274.2 471 Missense Mutation XP_005272331.1
XM_011513439.1 471 Intron XP_011511741.1
XM_011513443.1 471 Intron XP_011511745.1
XM_011513444.1 471 Missense Mutation XP_011511746.1
XM_011513445.2 471 Intron XP_011511747.1
XM_011513446.1 471 Missense Mutation XP_011511748.1
XM_017008039.1 471 Intron XP_016863528.1
XM_017008040.1 471 Intron XP_016863529.1
XM_017008041.1 471 Intron XP_016863530.1
XM_017008042.1 471 Intron XP_016863531.1

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