Product Details

SNP ID
rs140333389
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:80677234 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGGATAAATGAGATTTCTCTTTT[A/G]TTTCTTTTTTCTCTTTATCTTCTCC
Phenotype
MIM: 300553
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BRWD3 PubMed Links

Gene Details

Gene
BRWD3
Gene Name
bromodomain and WD repeat domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153252.4 5047 Missense Mutation ACA,ATA T1595I NP_694984.4
XM_005262113.3 5047 Missense Mutation ACA,ATA T1545I XP_005262170.1
XM_017029384.1 5047 Missense Mutation ACA,ATA T1191I XP_016884873.1
XM_017029385.1 5047 Intron XP_016884874.1

View Full Product Details