Product Details

SNP ID

rs3848596

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:33144855 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCGTTGATTTGAGGATCCGGTGGA[C/T]GGTTCTGTGGTTCGCGATTTTGAGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WDR88 PubMed Links

Gene Details

Gene

WDR88

Gene Name

WD repeat domain 88

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173479.3	471	Silent Mutation	GAC,GAT	D133D	NP_775750.3
XM_011526449.2	471	Silent Mutation	GAC,GAT	D133D	XP_011524751.1
XM_011526450.2	471	Silent Mutation	GAC,GAT	D133D	XP_011524752.1
XM_017026282.1	471	Silent Mutation	GAC,GAT	D133D	XP_016881771.1
XM_017026283.1	471	Silent Mutation	GAC,GAT	D133D	XP_016881772.1

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