Product Details

SNP ID
rs1051432
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.16:74873752 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GTCCATCAGCTCAGTAAATGTACCA[C/G]CTTCTAAAGCCATGATGCCATAGGT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
WDR59 PubMed Links

Gene Details

Gene
WDR59
Gene Name
WD repeat domain 59
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324171.1 3226 Intron NP_001311100.1
NM_001324172.1 3226 Intron NP_001311101.1
NM_030581.3 3226 UTR 3 NP_085058.3
XM_005256146.3 3226 UTR 3 XP_005256203.1
XM_011523331.2 3226 UTR 3 XP_011521633.1
XM_011523332.2 3226 UTR 3 XP_011521634.1
XM_017023667.1 3226 UTR 3 XP_016879156.1
XM_017023668.1 3226 UTR 3 XP_016879157.1
XM_017023669.1 3226 UTR 3 XP_016879158.1
XM_017023670.1 3226 UTR 3 XP_016879159.1

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