Product Details

SNP ID
rs114282947
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:159161323 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCAAGCTGCTCTTTCGTAGCAAT[A/G]GGTAACGATTTAATCTTATTCACAG
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RNF145 PubMed Links

Gene Details

Gene
RNF145
Gene Name
ring finger protein 145
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199380.1 1782 Silent Mutation CCC,CCT P553P NP_001186309.1
NM_001199381.1 1782 Silent Mutation CCC,CCT P540P NP_001186310.1
NM_001199382.1 1782 Silent Mutation CCC,CCT P537P NP_001186311.1
NM_001199383.1 1782 Silent Mutation CCC,CCT P523P NP_001186312.1
NM_144726.2 1782 Silent Mutation CCC,CCT P551P NP_653327.1
XM_017009138.1 1782 Silent Mutation CCC,CCT P523P XP_016864627.1

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