Product Details

SNP ID
rs188128205
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:156768218 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAAGAGCCCGTGAAGATCGCGGC[G/T]CCGGAGTTGCATAAGGGAGATGTGA
Phenotype
MIM: 179755
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
PRCC PubMed Links

Gene Details

Gene
PRCC
Gene Name
papillary renal cell carcinoma (translocation-associated)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005973.4 737 Silent Mutation GCG,GCT A149A NP_005964.3
XM_005245313.2 737 Silent Mutation GCG,GCT A149A XP_005245370.1
XM_005245314.1 737 Silent Mutation GCG,GCT A149A XP_005245371.1
XM_011509726.1 737 Silent Mutation GCG,GCT A149A XP_011508028.1

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