Product Details

SNP ID
rs141582392
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:51584801 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGTGATCGTGCCCAAAGAGGAGGG[C/T]GTCATCAGCGTCTCCGAGGACAGGT
Phenotype
MIM: 610418
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDFY2 PubMed Links

Gene Details

Gene
WDFY2
Gene Name
WD repeat and FYVE domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052950.3 345 Silent Mutation GGC,GGT G38G NP_443182.1
XM_011534914.1 345 Silent Mutation GGC,GGT G38G XP_011533216.1
XM_011534915.2 345 UTR 5 XP_011533217.1
XM_017020386.1 345 UTR 5 XP_016875875.1

View Full Product Details