Product Details

SNP ID
rs147454579
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:893082 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGTCCACGTGGAGGTGCATCAGCG[C/T]GGCAGCAGGTGAGCCGGACCTGTCC
Phenotype
MIM: 604507
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BRD9 PubMed Links

Gene Details

Gene
BRD9
Gene Name
bromodomain containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001009877.2 229 Intron NP_001009877.2
NM_001317951.1 229 Intron NP_001304880.1
NM_023924.4 229 Intron NP_076413.3
XM_006714494.3 229 Intron XP_006714557.1
XM_017009780.1 229 Intron XP_016865269.1
Gene
TRIP13
Gene Name
thyroid hormone receptor interactor 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166260.1 229 Silent Mutation CGC,CGT R28R NP_001159732.1
NM_004237.3 229 Silent Mutation CGC,CGT R28R NP_004228.1
XM_011514163.2 229 Silent Mutation CGC,CGT R28R XP_011512465.1

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