Product Details

SNP ID

rs201380094

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:5361185 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGGCTGGCTTCTTTTTTTTAATC[C/G]CTCTGTTTCAAGAATTAAAAGAAGA

Phenotype

Polymorphism

C/G, Transversion 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	496	Missense Mutation	GCG,GGG	A72G	NP_060935.2
XM_005251510.4	496	Missense Mutation	GCG,GGG	A72G	XP_005251567.1
XM_005251512.4	496	Missense Mutation	GCG,GGG	A39G	XP_005251569.1
XM_011517960.2	496	Missense Mutation	GCG,GGG	A72G	XP_011516262.1

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