Product Details

SNP ID

rs151159930

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:84677377 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAACTCGGCCTCGACTGTCACCAA[C/T]GAGGATCCTACTGTGATCCCTGCAG

Phenotype

Polymorphism

C/T, 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	10639	Missense Mutation	ATT,GTT	I3427V	NP_055806.2
XM_005262858.4	10639	Missense Mutation	ATT,GTT	I3445V	XP_005262915.1
XM_011531757.2	10639	Missense Mutation	ATT,GTT	I3445V	XP_011530059.1
XM_011531759.2	10639	Missense Mutation	ATT,GTT	I3445V	XP_011530061.1
XM_011531760.2	10639	Missense Mutation	ATT,GTT	I3445V	XP_011530062.1
XM_011531761.2	10639	Missense Mutation	ATT,GTT	I3430V	XP_011530063.1
XM_011531762.2	10639	Missense Mutation	ATT,GTT	I3428V	XP_011530064.1
XM_011531763.2	10639	Missense Mutation	ATT,GTT	I3427V	XP_011530065.1
XM_011531764.2	10639	Missense Mutation	ATT,GTT	I3417V	XP_011530066.1
XM_011531765.2	10639	Missense Mutation	ATT,GTT	I3410V	XP_011530067.1
XM_011531766.2	10639	Intron			XP_011530068.1
XM_011531767.2	10639	Intron			XP_011530069.1
XM_017007906.1	10639	Missense Mutation	ATT,GTT	I3445V	XP_016863395.1
XM_017007907.1	10639	Missense Mutation	ATT,GTT	I3445V	XP_016863396.1
XM_017007908.1	10639	Missense Mutation	ATT,GTT	I3445V	XP_016863397.1
XM_017007909.1	10639	Missense Mutation	ATT,GTT	I2767V	XP_016863398.1

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