Product Details
- SNP ID
-
rs146624359
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:49774372 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATCATCTTTAACTTGTCTATAGTT[C/T]CGTCAATACCAAGGGGAACCATTTT
- Phenotype
-
MIM: 604589
- Polymorphism
- C/T, Transition 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 |
2509 |
Missense Mutation |
GAA,GGA |
E1144G |
NP_001291737.1 |
NM_001304809.1 |
2509 |
Missense Mutation |
GAA,GGA |
E1013G |
NP_001291738.1 |
XM_011530073.1 |
2509 |
Missense Mutation |
GAA,GGA |
E739G |
XP_011528375.1 |
XM_017028714.1 |
2509 |
Missense Mutation |
GAA,GGA |
E1142G |
XP_016884203.1 |
XM_017028715.1 |
2509 |
Missense Mutation |
GAA,GGA |
E1144G |
XP_016884204.1 |
XM_017028716.1 |
2509 |
Missense Mutation |
GAA,GGA |
E1144G |
XP_016884205.1 |
XM_017028717.1 |
2509 |
Missense Mutation |
GAA,GGA |
E1144G |
XP_016884206.1 |
XM_017028718.1 |
2509 |
Missense Mutation |
GAA,GGA |
E978G |
XP_016884207.1 |
XM_017028719.1 |
2509 |
Intron |
|
|
XP_016884208.1 |
XM_017028720.1 |
2509 |
Intron |
|
|
XP_016884209.1 |
XM_017028721.1 |
2509 |
Intron |
|
|
XP_016884210.1 |
XM_017028722.1 |
2509 |
Missense Mutation |
GAA,GGA |
E757G |
XP_016884211.1 |
XM_017028723.1 |
2509 |
Missense Mutation |
GAA,GGA |
E598G |
XP_016884212.1 |
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