Product Details

SNP ID
rs143729485
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:58008687 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAACAAACGCATCGGCAACCTGCA[A/G]ACCGACCTGAGCGACGGGCTGCGGC
Phenotype
MIM: 603381
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FLNB PubMed Links

Gene Details

Gene
FLNB
Gene Name
filamin B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164317.1 288 Silent Mutation CAA,CAG Q41Q NP_001157789.1
NM_001164318.1 288 Silent Mutation CAA,CAG Q41Q NP_001157790.1
NM_001164319.1 288 Silent Mutation CAA,CAG Q41Q NP_001157791.1
NM_001457.3 288 Silent Mutation CAA,CAG Q41Q NP_001448.2
XM_005264978.1 288 Silent Mutation CAA,CAG Q41Q XP_005265035.1

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