Product Details

SNP ID

rs149937589

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:68131342 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGGACTCCAATCCAAACTTGAAA[C/T]GGGCTGGGTGGACAACGTAACATTC

Phenotype

MIM: 610729

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WDR92 PubMed Links

Gene Details

Gene

WDR92

Gene Name

WD repeat domain 92

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256476.1	1087	Intron			NP_001243405.1
NM_138458.3	1087	Missense Mutation	ATT,GTT	I324V	NP_612467.1

View Full Product Details