Product Details

SNP ID
rs34606154
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:100258815 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAAGAATGTTAACAGTAGCAAAG[C/T]GGGTGTGATAATCACTGGAACCATG
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 2431 Missense Mutation CAC,CGC H753R NP_001267468.1
NM_015435.4 2431 Missense Mutation CAC,CGC H753R NP_056250.3
NM_183419.3 2431 Missense Mutation CAC,CGC H753R NP_904355.1
XM_005250853.3 2431 Missense Mutation CAC,CGC H753R XP_005250910.1
XM_011516956.2 2431 Missense Mutation CAC,CGC H699R XP_011515258.1
XM_017013302.1 2431 Missense Mutation CAC,CGC H753R XP_016868791.1
XM_017013303.1 2431 Missense Mutation CAC,CGC H753R XP_016868792.1
XM_017013304.1 2431 Missense Mutation CAC,CGC H699R XP_016868793.1
XM_017013305.1 2431 Missense Mutation CAC,CGC H443R XP_016868794.1

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