Product Details

SNP ID

rs199638108

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:35174910 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTGCAGTCCTACCTGCTCCAGTT[C/G]CACGGCCTCGTGCGCCTGGTGCACC

Phenotype

MIM: 600646

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PROCR PubMed Links

Gene Details

Gene

PROCR

Gene Name

protein C receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006404.4	497	Missense Mutation	TTC,TTG	F93L	NP_006395.2
XM_011528496.1	497	Missense Mutation	TTC,TTG	F93L	XP_011526798.1

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