Product Details

SNP ID
rs149813610
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:896743 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGATGGCCCCAGCAGTGAAAATCTG[C/G]AGGAAGAGACAGAAAACATAATTGC
Phenotype
MIM: 604507
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BRD9 PubMed Links

Gene Details

Gene
BRD9
Gene Name
bromodomain containing 9
There are no transcripts associated with this gene.

Gene
TRIP13
Gene Name
thyroid hormone receptor interactor 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166260.1 482 Missense Mutation CAG,GAG Q113E NP_001159732.1
NM_004237.3 482 Missense Mutation CAG,GAG Q113E NP_004228.1
XM_011514163.2 482 Missense Mutation CAG,GAG Q113E XP_011512465.1

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