Product Details

SNP ID
rs961498
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:107319734 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCCCCGGAGCTGCAGTGGCCCTG[C/G]GTCAGGCTCGGGCTCCGGCCCAGGC
Phenotype
Polymorphism
C/G, 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 2567 Intron NP_001017523.1
NM_001018072.1 2567 Missense Mutation GCG,GGG A265G NP_001018082.1
XM_005268645.3 2567 Intron XP_005268702.1
XM_011537909.2 2567 Intron XP_011536211.1
XM_011537910.2 2567 Intron XP_011536212.1
XM_017018807.1 2567 Missense Mutation GCG,GGG A265G XP_016874296.1

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