Product Details

SNP ID

rs199786557

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:5358261 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTCATTTGTCTATGAAGAATCTA[C/T]TCTGTTCCTTTCTGGCTTTTTCAAT

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	703	Missense Mutation	AAT,AGT	N141S	NP_060935.2
XM_005251510.4	703	Missense Mutation	AAT,AGT	N141S	XP_005251567.1
XM_005251512.4	703	Missense Mutation	AAT,AGT	N108S	XP_005251569.1
XM_011517960.2	703	Missense Mutation	AAT,AGT	N141S	XP_011516262.1

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