Product Details

SNP ID
rs3765224
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:169426594 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTACCGTGCCAATTGAGTTCTGC[A/G]AGAGCCACTGGAAGCTCGCCGTGAC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC401287 PubMed Links

Gene Details

Gene
LOC401287
Gene Name
uncharacterized LOC401287
There are no transcripts associated with this gene.

Gene
WDR27
Gene Name
WD repeat domain 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202550.1 4420 Intron NP_001189479.1
NM_182552.4 4420 Intron NP_872358.4
XM_011535682.2 4420 Intron XP_011533984.1
XM_011535684.2 4420 Intron XP_011533986.1
XM_011535685.2 4420 Intron XP_011533987.1
XM_011535687.2 4420 UTR 3 XP_011533989.1
XM_011535688.2 4420 UTR 3 XP_011533990.1
XM_011535689.2 4420 UTR 3 XP_011533991.1
XM_011535690.2 4420 Intron XP_011533992.1
XM_011535691.2 4420 Intron XP_011533993.1
XM_011535692.2 4420 Intron XP_011533994.1
XM_011535693.2 4420 Intron XP_011533995.1
XM_011535694.2 4420 Intron XP_011533996.1
XM_011535696.2 4420 Intron XP_011533998.1
XM_011535697.2 4420 Intron XP_011533999.1
XM_017010658.1 4420 Intron XP_016866147.1
XM_017010659.1 4420 Intron XP_016866148.1
XM_017010660.1 4420 Intron XP_016866149.1
XM_017010661.1 4420 UTR 3 XP_016866150.1
XM_017010662.1 4420 Intron XP_016866151.1
XM_017010663.1 4420 Intron XP_016866152.1
XM_017010664.1 4420 Intron XP_016866153.1
XM_017010665.1 4420 Intron XP_016866154.1
XM_017010666.1 4420 Intron XP_016866155.1
XM_017010667.1 4420 Intron XP_016866156.1
XM_017010668.1 4420 Intron XP_016866157.1
XM_017010669.1 4420 Intron XP_016866158.1
XM_017010670.1 4420 Intron XP_016866159.1
XM_017010671.1 4420 Intron XP_016866160.1
XM_017010672.1 4420 Intron XP_016866161.1
XM_017010673.1 4420 Intron XP_016866162.1
XM_017010674.1 4420 Intron XP_016866163.1
XM_017010675.1 4420 Intron XP_016866164.1

View Full Product Details