Product Details

SNP ID
rs200101252
Assay Type
Functionally tested
NCBI dbSNP Submissions
13
Location
Chr.1:222725496 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTACACCTGCGGAAAAAGGAAGAG[A/C]TTTAGAGTCACGACTCATAGAAGCA
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
BROX PubMed Links

Gene Details

Gene
BROX
Gene Name
BRO1 domain and CAAX motif containing
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288579.1 996 Missense Mutation GAT,GCT D142A NP_001275508.1
NM_001288580.1 996 Missense Mutation GAT,GCT D142A NP_001275509.1
NM_001288581.1 996 Missense Mutation GAT,GCT D174A NP_001275510.1
NM_144695.3 996 Missense Mutation GAT,GCT D174A NP_653296.2
XM_005273065.2 996 Missense Mutation GAT,GCT D174A XP_005273122.2
XM_005273069.4 996 Missense Mutation GAT,GCT D119A XP_005273126.1
XM_006711173.3 996 Missense Mutation GAT,GCT D191A XP_006711236.1
XM_011509212.2 996 Missense Mutation GAT,GCT D195A XP_011507514.1
XM_011509213.2 996 Missense Mutation GAT,GCT D188A XP_011507515.1
XM_011509214.2 996 Missense Mutation GAT,GCT D174A XP_011507516.1
XM_017000374.1 996 Missense Mutation GAT,GCT D174A XP_016855863.1
XM_017000375.1 996 Missense Mutation GAT,GCT D156A XP_016855864.1
XM_017000376.1 996 Missense Mutation GAT,GCT D119A XP_016855865.1

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