Product Details

SNP ID
rs147728519
Assay Type
Functionally Tested
NCBI dbSNP Submissions
11
Location
Chr.1:32633978 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGTTTCTACTTCTACTGTTTGGA[A/G]GGGCTCCACTGTCCCAGTATCTGTC
Phenotype
MIM: 615891
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ZBTB8OS PubMed Links

Gene Details

Gene
ZBTB8OS
Gene Name
zinc finger and BTB domain containing 8 opposite strand
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308135.1 257 Missense Mutation CTC,TTC L78F NP_001295064.1
NM_001308136.1 257 Missense Mutation CTC,TTC L85F NP_001295065.1
NM_001308137.1 257 Missense Mutation CTC,TTC L78F NP_001295066.1
NM_001308138.1 257 Missense Mutation CTC,TTC L16F NP_001295067.1
NM_001308139.1 257 Missense Mutation CTC,TTC L16F NP_001295068.1
NM_001308140.1 257 Missense Mutation CTC,TTC L16F NP_001295069.1
NM_001308141.1 257 Missense Mutation CTC,TTC L16F NP_001295070.1
NM_178547.3 257 Missense Mutation CTC,TTC L85F NP_848642.1
XM_011541327.2 257 Missense Mutation CTC,TTC L85F XP_011539629.1
XM_011541328.1 257 Intron XP_011539630.1
XM_011541329.2 257 Missense Mutation CTC,TTC L37F XP_011539631.1
XM_011541330.2 257 Missense Mutation CTC,TTC L33F XP_011539632.1
XM_011541334.2 257 Missense Mutation CTC,TTC L16F XP_011539636.1
XM_011541335.2 257 Intron XP_011539637.1
XM_011541337.2 257 Intron XP_011539639.1
XM_011541338.2 257 Missense Mutation CTC,TTC L16F XP_011539640.1
XM_017001134.1 257 Intron XP_016856623.1
XM_017001135.1 257 Missense Mutation CTC,TTC L85F XP_016856624.1
XM_017001136.1 257 Intron XP_016856625.1
XM_017001137.1 257 Intron XP_016856626.1
XM_017001138.1 257 Missense Mutation CTC,TTC L16F XP_016856627.1

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