Product Details

SNP ID
rs199720664
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:91962765 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAAAGCAGTTAAGAATGTCTCTGC[C/G]AAGTCGACAAACAGCTATTATTGTT
Phenotype
MIM: 602144
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BRDT PubMed Links

Gene Details

Gene
BRDT
Gene Name
bromodomain testis associated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242805.2 243 Missense Mutation CCA,CGA P4R NP_001229734.2
NM_001242806.2 243 Missense Mutation CCA,CGA P4R NP_001229735.2
NM_001242807.2 243 Missense Mutation CCA,CGA P4R NP_001229736.2
NM_001242808.2 243 Missense Mutation CCA,CGA P4R NP_001229737.2
NM_001242810.2 243 Intron NP_001229739.2
NM_001726.4 243 Missense Mutation CCA,CGA P4R NP_001717.3
NM_207189.3 243 Missense Mutation CCA,CGA P4R NP_997072.2
XM_006710853.3 243 Missense Mutation CCA,CGA P4R XP_006710916.1
XM_006710854.3 243 Missense Mutation CCA,CGA P4R XP_006710917.1
XM_006710855.3 243 Missense Mutation CCA,CGA P4R XP_006710918.1
XM_006710856.3 243 Missense Mutation CCA,CGA P4R XP_006710919.1
XM_006710857.3 243 Missense Mutation CCA,CGA P4R XP_006710920.1
XM_011542032.2 243 Missense Mutation CCA,CGA P4R XP_011540334.1
XM_011542033.2 243 Missense Mutation CCA,CGA P4R XP_011540335.1
XM_011542034.2 243 Missense Mutation CCA,CGA P4R XP_011540336.1
XM_011542035.2 243 Missense Mutation CCA,CGA P4R XP_011540337.1
XM_011542036.2 243 Missense Mutation CCA,CGA P4R XP_011540338.1

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