Product Details

SNP ID
rs35177403
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:100258634 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTATTTGTTTCTTTTAGTGCATC[A/G]CCAAAATATAAATCAACATTAGGTT
Phenotype
MIM: 607119
Polymorphism
A/G, 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 2612 Silent Mutation GGC,GGT G813G NP_001267468.1
NM_015435.4 2612 Silent Mutation GGC,GGT G813G NP_056250.3
NM_183419.3 2612 Silent Mutation GGC,GGT G813G NP_904355.1
XM_005250853.3 2612 Silent Mutation GGC,GGT G813G XP_005250910.1
XM_011516956.2 2612 Silent Mutation GGC,GGT G759G XP_011515258.1
XM_017013302.1 2612 Silent Mutation GGC,GGT G813G XP_016868791.1
XM_017013303.1 2612 Silent Mutation GGC,GGT G813G XP_016868792.1
XM_017013304.1 2612 Silent Mutation GGC,GGT G759G XP_016868793.1
XM_017013305.1 2612 Silent Mutation GGC,GGT G503G XP_016868794.1

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