Product Details

SNP ID
rs151226712
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:100258957 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGGGATGGAGCCTCAAATTCAC[C/T]TGAGTTCGTGCTTTGTTGTTCTAAC
Phenotype
MIM: 607119
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF19A PubMed Links

Gene Details

Gene
RNF19A
Gene Name
ring finger protein 19A, RBR E3 ubiquitin protein ligase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001280539.1 2289 Missense Mutation AGT,GGT S706G NP_001267468.1
NM_015435.4 2289 Missense Mutation AGT,GGT S706G NP_056250.3
NM_183419.3 2289 Missense Mutation AGT,GGT S706G NP_904355.1
XM_005250853.3 2289 Missense Mutation AGT,GGT S706G XP_005250910.1
XM_011516956.2 2289 Missense Mutation AGT,GGT S652G XP_011515258.1
XM_017013302.1 2289 Missense Mutation AGT,GGT S706G XP_016868791.1
XM_017013303.1 2289 Missense Mutation AGT,GGT S706G XP_016868792.1
XM_017013304.1 2289 Missense Mutation AGT,GGT S652G XP_016868793.1
XM_017013305.1 2289 Missense Mutation AGT,GGT S396G XP_016868794.1

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