Product Details

SNP ID
rs145569116
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:9810937 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGACTCTTTGGGGCAAGCCCTGA[C/T]GATGACCATACAGTGGGGCAGCCCC
Phenotype
MIM: 609079
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXL12 PubMed Links

Gene Details

Gene
FBXL12
Gene Name
F-box and leucine rich repeat protein 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001316936.1 1230 Missense Mutation NP_001303865.1
NM_001316937.1 1230 Missense Mutation NP_001303866.1
NM_001316938.1 1230 Missense Mutation NP_001303867.1
NM_001316939.1 1230 Missense Mutation NP_001303868.1
NM_001316940.1 1230 Missense Mutation NP_001303869.1
NM_001316941.1 1230 Missense Mutation NP_001303870.1
NM_001316942.1 1230 Missense Mutation NP_001303871.1
NM_017703.2 1230 Missense Mutation NP_060173.1
XM_006722782.3 1230 Missense Mutation XP_006722845.2
XM_017026912.1 1230 Missense Mutation XP_016882401.1

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