Product Details

SNP ID
rs145688334
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:107319436 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCAAGTACGAGATCCAGAGCGCC[A/C]TGGAGATCGTGCTGTCCTGGGGCCT
Phenotype
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
BTBD11 PubMed Links

Gene Details

Gene
BTBD11
Gene Name
BTB domain containing 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001017523.1 2269 Intron NP_001017523.1
NM_001018072.1 2269 Missense Mutation ATG,CTG M166L NP_001018082.1
XM_005268645.3 2269 Intron XP_005268702.1
XM_011537909.2 2269 Intron XP_011536211.1
XM_011537910.2 2269 Intron XP_011536212.1
XM_017018807.1 2269 Missense Mutation ATG,CTG M166L XP_016874296.1

View Full Product Details