Product Details
- SNP ID
-
rs143497188
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:129840313 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAGGCTTGGGGCCGGACCACGGGC[A/G]CGAAGGCGCTCTTCTGTTTCACTGC
- Phenotype
-
MIM: 607407
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
EBF3
PubMed Links
Gene Details
- Gene
- EBF3
- Gene Name
- early B-cell factor 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001005463.2 |
1191 |
Missense Mutation |
GCG,GTG |
A519V |
NP_001005463.1 |
XM_005252667.3 |
1191 |
Missense Mutation |
GCG,GTG |
A555V |
XP_005252724.1 |
XM_005252668.3 |
1191 |
Missense Mutation |
GCG,GTG |
A564V |
XP_005252725.1 |
XM_005252669.3 |
1191 |
Missense Mutation |
GCG,GTG |
A555V |
XP_005252726.1 |
XM_006717739.3 |
1191 |
Missense Mutation |
GCG,GTG |
A564V |
XP_006717802.1 |
XM_006717740.3 |
1191 |
Missense Mutation |
GCG,GTG |
A563V |
XP_006717803.1 |
XM_006717741.3 |
1191 |
Missense Mutation |
GCG,GTG |
A564V |
XP_006717804.1 |
XM_006717742.3 |
1191 |
Missense Mutation |
GCG,GTG |
A528V |
XP_006717805.1 |
XM_006717743.3 |
1191 |
Missense Mutation |
GCG,GTG |
A528V |
XP_006717806.1 |
XM_006717744.3 |
1191 |
Missense Mutation |
GCG,GTG |
A465V |
XP_006717807.1 |
XM_011539574.2 |
1191 |
Missense Mutation |
GCG,GTG |
A469V |
XP_011537876.1 |
XM_011539575.2 |
1191 |
Missense Mutation |
GCG,GTG |
A392V |
XP_011537877.1 |
XM_017016027.1 |
1191 |
Missense Mutation |
GCG,GTG |
A465V |
XP_016871516.1 |
- Gene
- MIR4297
- Gene Name
- microRNA 4297
There are no transcripts associated with this gene.
View Full Product Details