Product Details

SNP ID

rs181154367

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:66814175 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGATCCAAGCAAAGTATCCATTAT[A/G]TCTCCCTGAAAAAAAAAAGTCACAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WDR78 PubMed Links

Gene Details

Gene

WDR78

Gene Name

WD repeat domain 78

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024763.4	2316	Silent Mutation	GAC,GAT	D834D	NP_079039.4
NM_207014.2	2316	Intron			NP_996897.2
XM_005271212.3	2316	Silent Mutation	GAC,GAT	D769D	XP_005271269.1
XM_011542161.2	2316	Silent Mutation	GAC,GAT	D805D	XP_011540463.1
XM_011542162.2	2316	Silent Mutation	GAC,GAT	D801D	XP_011540464.1
XM_017002353.1	2316	Silent Mutation	GAC,GAT	D736D	XP_016857842.1
XM_017002354.1	2316	Silent Mutation	GAC,GAT	D707D	XP_016857843.1
XM_017002355.1	2316	Silent Mutation	GAC,GAT	D580D	XP_016857844.1
XM_017002356.1	2316	Silent Mutation	GAC,GAT	D545D	XP_016857845.1
XM_017002357.1	2316	Intron			XP_016857846.1

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