Product Details

SNP ID

rs146420040

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:35176182 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTATCCACAGTTCCTCTGACCATC[C/T]GCTGCTTCCTGGGCTGTGAGCTGCC

Phenotype

MIM: 600646

Polymorphism

C/T, Transition 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	555	Missense Mutation	CGC,TGC	R113C	NP_006395.2
XM_011528496.1	555	Missense Mutation	CGC,TGC	R113C	XP_011526798.1

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