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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