Product Details
- SNP ID
-
rs146936488
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:190098799 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATAAAAATGGCATGGACTTCTATT[C/T]GTCTGTCCGTTTTCTGCAGCAGATA
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
BRINP3
PubMed Links
Gene Details
- Gene
- BRINP3
- Gene Name
- BMP/retinoic acid inducible neural specific 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001317188.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q405R |
NP_001304117.1 |
NM_199051.2 |
2095 |
Missense Mutation |
CAA,CGA |
Q507R |
NP_950252.1 |
XM_011509472.2 |
2095 |
Missense Mutation |
CAA,CGA |
Q477R |
XP_011507774.1 |
XM_011509475.2 |
2095 |
Missense Mutation |
CAA,CGA |
Q464R |
XP_011507777.1 |
XM_011509476.2 |
2095 |
Missense Mutation |
CAA,CGA |
Q405R |
XP_011507778.1 |
XM_017001125.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q507R |
XP_016856614.1 |
XM_017001126.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q507R |
XP_016856615.1 |
XM_017001127.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q477R |
XP_016856616.1 |
XM_017001128.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q477R |
XP_016856617.1 |
XM_017001129.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q405R |
XP_016856618.1 |
XM_017001130.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q405R |
XP_016856619.1 |
XM_017001131.1 |
2095 |
Missense Mutation |
CAA,CGA |
Q214R |
XP_016856620.1 |
XM_017001132.1 |
2095 |
Intron |
|
|
XP_016856621.1 |
XM_017001133.1 |
2095 |
Intron |
|
|
XP_016856622.1 |
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