Product Details

SNP ID
rs141626867
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48372800 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCGATTGCCTGACTTAGCTTTGAA[C/G]CGAATCTTCTCTTTCCTGGACCTGT
Phenotype
MIM: 609075
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
FBXW12 PubMed Links

Gene Details

Gene
FBXW12
Gene Name
F-box and WD repeat domain containing 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001159927.1 232 Missense Mutation AAC,AAG N11K NP_001153399.1
NM_001159929.1 232 Intron NP_001153401.1
NM_207102.2 232 Missense Mutation AAC,AAG N11K NP_996985.2
XM_017006224.1 232 Missense Mutation AAC,AAG N11K XP_016861713.1

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