Product Details

SNP ID

rs148734945

Assay Type

Functionally tested

NCBI dbSNP Submissions

23

Location

Chr.1:66814152 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATTATGCTGATTGGTTTGACTTG[A/G]ATCCAAGCAAAGTATCCATTATATC

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	2339	Missense Mutation	TCC,TTC	S842F	NP_079039.4
NM_207014.2	2339	Intron			NP_996897.2
XM_005271212.3	2339	Missense Mutation	TCC,TTC	S777F	XP_005271269.1
XM_011542161.2	2339	Missense Mutation	TCC,TTC	S813F	XP_011540463.1
XM_011542162.2	2339	Missense Mutation	TCC,TTC	S809F	XP_011540464.1
XM_017002353.1	2339	Missense Mutation	TCC,TTC	S744F	XP_016857842.1
XM_017002354.1	2339	Missense Mutation	TCC,TTC	S715F	XP_016857843.1
XM_017002355.1	2339	Missense Mutation	TCC,TTC	S588F	XP_016857844.1
XM_017002356.1	2339	Missense Mutation	TCC,TTC	S553F	XP_016857845.1
XM_017002357.1	2339	Intron			XP_016857846.1

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