Product Details

SNP ID

rs201436617

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37885153 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAACAGGCAGCAGAACAGCCGTT[A/C]CCCGGGAACTAGCTCTGTGGCTTTT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

WDR87 PubMed Links

Gene Details

Gene

WDR87

Gene Name

WD repeat domain 87

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291088.1	8772	Missense Mutation			NP_001278017.1
NM_031951.4	8772	Missense Mutation			NP_114157.4
XM_011527360.2	8772	Nonsense Mutation			XP_011525662.1

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