Product Details

SNP ID
rs201066160
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:83257837 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAATGGCTGCTACTCTCTGACTTCA[C/T]GCTCGAGGTAGTGCTCAAATCCAGG
Phenotype
MIM: 601930
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BNC1 PubMed Links

Gene Details

Gene
BNC1
Gene Name
basonuclin 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301206.1 2814 Missense Mutation ATG,GTG M857V NP_001288135.1
NM_001717.3 2814 Missense Mutation ATG,GTG M864V NP_001708.3
XM_011521893.1 2814 Missense Mutation ATG,GTG M839V XP_011520195.1
XM_011521894.1 2814 Missense Mutation ATG,GTG M746V XP_011520196.1

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