Product Details

SNP ID
rs150282383
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:120546544 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTAACAAGATGCCTCCTCAAAG[A/G]GGCGGCGGCAGCAGCAAACTCTTTA
Phenotype
MIM: 615998
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF10 PubMed Links

Gene Details

Gene
RNF10
Gene Name
ring finger protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014868.4 800 Silent Mutation AGA,AGG R99R NP_055683.3
XM_005254013.2 800 Silent Mutation AGA,AGG R49R XP_005254070.1
XM_006719717.2 800 Silent Mutation AGA,AGG R99R XP_006719780.1
XM_017020282.1 800 Silent Mutation AGA,AGG R49R XP_016875771.1
XM_017020283.1 800 Silent Mutation AGA,AGG R99R XP_016875772.1

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