Product Details

SNP ID

rs143489829

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:103100307 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCACAGACTCCAGCTCAGGGCTCC[C/T]GGCGAACAAGCAGCAGGAAAGAGCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

EXOC3L4 PubMed Links

Gene Details

Gene

EXOC3L4

Gene Name

exocyst complex component 3 like 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077594.1	571	Missense Mutation	CGG,TGG	R30W	NP_001071062.1
XM_011537323.2	571	Missense Mutation	CGG,TGG	R88W	XP_011535625.1
XM_011537324.2	571	Missense Mutation	CGG,TGG	R88W	XP_011535626.1
XM_011537325.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535627.1
XM_011537327.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535629.1
XM_011537328.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535630.1
XM_011537329.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535631.1
XM_011537330.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535632.1
XM_011537331.1	571	Missense Mutation	CGG,TGG	R30W	XP_011535633.1
XM_011537332.2	571	Missense Mutation	CGG,TGG	R30W	XP_011535634.1
XM_011537333.2	571	Missense Mutation	CGG,TGG	R67W	XP_011535635.1
XM_011537334.1	571	Intron			XP_011535636.1

View Full Product Details