Product Details

SNP ID

rs149067356

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:84672963 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCACCGGGGATGAGATTTTCAAGC[A/G]TTTGATTTCAGATTGAAAGCGACTG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WDFY3 PubMed Links

Gene Details

Gene

WDFY3

Gene Name

WD repeat and FYVE domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014991.4	10846	Missense Mutation	CGC,TGC	R3496C	NP_055806.2
XM_005262858.4	10846	Missense Mutation	CGC,TGC	R3514C	XP_005262915.1
XM_011531757.2	10846	Missense Mutation	CGC,TGC	R3514C	XP_011530059.1
XM_011531759.2	10846	Missense Mutation	CGC,TGC	R3514C	XP_011530061.1
XM_011531760.2	10846	Missense Mutation	CGC,TGC	R3514C	XP_011530062.1
XM_011531761.2	10846	Missense Mutation	CGC,TGC	R3499C	XP_011530063.1
XM_011531762.2	10846	Missense Mutation	CGC,TGC	R3497C	XP_011530064.1
XM_011531763.2	10846	Missense Mutation	CGC,TGC	R3496C	XP_011530065.1
XM_011531764.2	10846	Missense Mutation	CGC,TGC	R3486C	XP_011530066.1
XM_011531765.2	10846	Missense Mutation	CGC,TGC	R3479C	XP_011530067.1
XM_011531766.2	10846	Intron			XP_011530068.1
XM_011531767.2	10846	Intron			XP_011530069.1
XM_017007906.1	10846	Missense Mutation	CGC,TGC	R3514C	XP_016863395.1
XM_017007907.1	10846	Missense Mutation	CGC,TGC	R3514C	XP_016863396.1
XM_017007908.1	10846	Missense Mutation	CGC,TGC	R3514C	XP_016863397.1
XM_017007909.1	10846	Missense Mutation	CGC,TGC	R2836C	XP_016863398.1

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