Product Details

SNP ID
rs151186096
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:80677112 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCTATAATCATGGTCTCCATCTA[C/T]GTAATCTTGATCTGTTCTGGAAGTT
Phenotype
MIM: 300553
Polymorphism
C/T, 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 5169 Missense Mutation ATA,GTA I1636V NP_694984.4
XM_005262113.3 5169 Missense Mutation ATA,GTA I1586V XP_005262170.1
XM_017029384.1 5169 Missense Mutation ATA,GTA I1232V XP_016884873.1
XM_017029385.1 5169 Intron XP_016884874.1

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