Product Details

SNP ID
rs13202383
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:169426449 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACAAGCCCCTTATTAACTTTATTA[A/G]AGGTTAACCGTCTCAAATTTACAGT
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 4565 Intron NP_001189479.1
NM_182552.4 4565 Intron NP_872358.4
XM_011535682.2 4565 Intron XP_011533984.1
XM_011535684.2 4565 Intron XP_011533986.1
XM_011535685.2 4565 Intron XP_011533987.1
XM_011535687.2 4565 UTR 3 XP_011533989.1
XM_011535688.2 4565 UTR 3 XP_011533990.1
XM_011535689.2 4565 UTR 3 XP_011533991.1
XM_011535690.2 4565 Intron XP_011533992.1
XM_011535691.2 4565 Intron XP_011533993.1
XM_011535692.2 4565 Intron XP_011533994.1
XM_011535693.2 4565 Intron XP_011533995.1
XM_011535694.2 4565 Intron XP_011533996.1
XM_011535696.2 4565 Intron XP_011533998.1
XM_011535697.2 4565 Intron XP_011533999.1
XM_017010658.1 4565 Intron XP_016866147.1
XM_017010659.1 4565 Intron XP_016866148.1
XM_017010660.1 4565 Intron XP_016866149.1
XM_017010661.1 4565 UTR 3 XP_016866150.1
XM_017010662.1 4565 Intron XP_016866151.1
XM_017010663.1 4565 Intron XP_016866152.1
XM_017010664.1 4565 Intron XP_016866153.1
XM_017010665.1 4565 Intron XP_016866154.1
XM_017010666.1 4565 Intron XP_016866155.1
XM_017010667.1 4565 Intron XP_016866156.1
XM_017010668.1 4565 Intron XP_016866157.1
XM_017010669.1 4565 Intron XP_016866158.1
XM_017010670.1 4565 Intron XP_016866159.1
XM_017010671.1 4565 Intron XP_016866160.1
XM_017010672.1 4565 Intron XP_016866161.1
XM_017010673.1 4565 Intron XP_016866162.1
XM_017010674.1 4565 Intron XP_016866163.1
XM_017010675.1 4565 Intron XP_016866164.1

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