Product Details
- SNP ID
-
rs151282207
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:49774260 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTCAATGTCACTGAGGTCGCTGGT[A/C]GGCTCCCCGTGGACGCGGCTCAGGT
- Phenotype
-
MIM: 604589
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
BRD1
PubMed Links
Gene Details
- Gene
- BRD1
- Gene Name
- bromodomain containing 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001304808.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1181P |
NP_001291737.1 |
| NM_001304809.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1050P |
NP_001291738.1 |
| XM_011530073.1 |
2621 |
Silent Mutation |
CCG,CCT |
P776P |
XP_011528375.1 |
| XM_017028714.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1179P |
XP_016884203.1 |
| XM_017028715.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1181P |
XP_016884204.1 |
| XM_017028716.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1181P |
XP_016884205.1 |
| XM_017028717.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1181P |
XP_016884206.1 |
| XM_017028718.1 |
2621 |
Silent Mutation |
CCG,CCT |
P1015P |
XP_016884207.1 |
| XM_017028719.1 |
2621 |
Intron |
|
|
XP_016884208.1 |
| XM_017028720.1 |
2621 |
Intron |
|
|
XP_016884209.1 |
| XM_017028721.1 |
2621 |
Intron |
|
|
XP_016884210.1 |
| XM_017028722.1 |
2621 |
Silent Mutation |
CCG,CCT |
P794P |
XP_016884211.1 |
| XM_017028723.1 |
2621 |
Silent Mutation |
CCG,CCT |
P635P |
XP_016884212.1 |
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