Product Details

SNP ID
rs200950423
Assay Type
Functionally tested
NCBI dbSNP Submissions
8
Location
Chr.1:156768015 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGACCCCAGGCTTCAGCCTCCTCCC[C/G]CCTTGCCCTTCGGCCTGGGAGGCTT
Phenotype
MIM: 179755
Polymorphism
C/G, 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_005973.4 534 Missense Mutation CCC,GCC P82A NP_005964.3
XM_005245313.2 534 Missense Mutation CCC,GCC P82A XP_005245370.1
XM_005245314.1 534 Missense Mutation CCC,GCC P82A XP_005245371.1
XM_011509726.1 534 Missense Mutation CCC,GCC P82A XP_011508028.1

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