Product Details

SNP ID

rs11545731

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:156767615 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGTTCGGTGGAAATCAGCCGTAG[C/T]CATGAGTTTCTGCCGGGGCTAGCCC

Phenotype

MIM: 179755

Polymorphism

C/T, Transition 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	134	UTR 5			NP_005964.3
XM_005245313.2	134	UTR 5			XP_005245370.1
XM_005245314.1	134	UTR 5			XP_005245371.1
XM_011509726.1	134	UTR 5			XP_011508028.1

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