Product Details

SNP ID
rs138921537
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:83257570 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTACTTTGCATTTGTGGAGCTGCC[A/G]GAGGTGCACAGTTTTGTAGTGGGCC
Phenotype
MIM: 601930
Polymorphism
A/G, 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 3081 Missense Mutation CGG,TGG R946W NP_001288135.1
NM_001717.3 3081 Missense Mutation CGG,TGG R953W NP_001708.3
XM_011521893.1 3081 Missense Mutation CGG,TGG R928W XP_011520195.1
XM_011521894.1 3081 Missense Mutation CGG,TGG R835W XP_011520196.1

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