Product Details

SNP ID
rs201697023
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:74874270 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGGTGGGACACACCTCCTGGGTC[C/T]GAAACCACTCCATCATGTGGCTGGT
Phenotype
Polymorphism
C/T, Transition 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 2708 Intron NP_001311100.1
NM_001324172.1 2708 Intron NP_001311101.1
NM_030581.3 2708 Missense Mutation CAG,CGG Q955R NP_085058.3
XM_005256146.3 2708 Missense Mutation CAG,CGG Q974R XP_005256203.1
XM_011523331.2 2708 Missense Mutation CAG,CGG Q667R XP_011521633.1
XM_011523332.2 2708 Missense Mutation CAG,CGG Q653R XP_011521634.1
XM_017023667.1 2708 Missense Mutation CAG,CGG Q703R XP_016879156.1
XM_017023668.1 2708 Missense Mutation CAG,CGG Q703R XP_016879157.1
XM_017023669.1 2708 Missense Mutation CAG,CGG Q667R XP_016879158.1
XM_017023670.1 2708 Missense Mutation CAG,CGG Q653R XP_016879159.1

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