Product Details

SNP ID
rs112013549
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:5361078 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAACTCTAGTTTACCAAAGACTTAC[C/T]TTTCATTCTTTCTAAAAGGGTTCCA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PLGRKT PubMed Links

Gene Details

Gene
PLGRKT
Gene Name
plasminogen receptor with a C-terminal lysine
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018465.3 603 Missense Mutation AGT,GGT S108G NP_060935.2
XM_005251510.4 603 Missense Mutation AGT,GGT S108G XP_005251567.1
XM_005251512.4 603 Missense Mutation AGT,GGT S75G XP_005251569.1
XM_011517960.2 603 Missense Mutation AGT,GGT S108G XP_011516262.1

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