Product Details

SNP ID
rs201881212
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:1634220 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCAGGAGCCTAGGGCTTTTCCTCC[A/G]CCCTCTTCTGTAAGCAGACTGGACA
Phenotype
MIM: 605158
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PXDN PubMed Links

Gene Details

Gene
PXDN
Gene Name
peroxidasin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012293.2 4516 Missense Mutation NP_036425.1
XM_005264707.3 4516 Missense Mutation XP_005264764.1
XM_011510396.1 4516 Missense Mutation XP_011508698.1
XM_011510397.2 4516 Missense Mutation XP_011508699.1

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