Product Details

SNP ID

rs202165364

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:51320014 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACAAATCTCCACCACACAGGTGAC[A/C]TGGCCACTCTGAAAGGCAGCATGCA

Phenotype

MIM: 615904

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

PXDNL PubMed Links

Gene Details

Gene

PXDNL

Gene Name

peroxidasin like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144651.4	5668	Missense Mutation			NP_653252.3
XM_005251168.3	5668	Missense Mutation			XP_005251225.1
XM_006716420.3	5668	Missense Mutation			XP_006716483.1
XM_011517456.2	5668	Missense Mutation			XP_011515758.1
XM_011517457.2	5668	Missense Mutation			XP_011515759.1
XM_011517458.2	5668	Missense Mutation			XP_011515760.1
XM_011517459.2	5668	Intron			XP_011515761.1
XM_017013041.1	5668	Missense Mutation			XP_016868530.1

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