Product Details
- SNP ID
-
rs201939465
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:1612362 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATCCCGCACGCGCACCCGCTCCCGC[A/G]CGTTATTGGCCATGCGCCTCTCCCG
- Phenotype
-
MIM: 147141
MIM: 609711
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TCF3
PubMed Links
Gene Details
- Gene
- TCF3
- Gene Name
- transcription factor 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001136139.2 |
1899 |
Missense Mutation |
GCG,GTG |
A553V |
NP_001129611.1 |
NM_003200.3 |
1899 |
Intron |
|
|
NP_003191.1 |
XM_006722852.3 |
1899 |
Intron |
|
|
XP_006722915.1 |
XM_006722853.3 |
1899 |
Intron |
|
|
XP_006722916.1 |
XM_006722855.3 |
1899 |
Missense Mutation |
GCG,GTG |
A582V |
XP_006722918.1 |
XM_006722856.3 |
1899 |
Missense Mutation |
GCG,GTG |
A582V |
XP_006722919.1 |
XM_006722857.3 |
1899 |
Missense Mutation |
GCG,GTG |
A581V |
XP_006722920.1 |
XM_006722858.3 |
1899 |
Missense Mutation |
GCG,GTG |
A581V |
XP_006722921.1 |
XM_011528215.2 |
1899 |
Intron |
|
|
XP_011526517.1 |
XM_011528216.2 |
1899 |
Intron |
|
|
XP_011526518.1 |
XM_011528217.2 |
1899 |
Intron |
|
|
XP_011526519.1 |
XM_011528219.2 |
1899 |
Intron |
|
|
XP_011526521.1 |
XM_011528220.2 |
1899 |
Missense Mutation |
GCG,GTG |
A582V |
XP_011526522.1 |
XM_011528221.2 |
1899 |
Missense Mutation |
GCG,GTG |
A581V |
XP_011526523.1 |
XM_011528223.2 |
1899 |
Intron |
|
|
XP_011526525.1 |
XM_011528225.2 |
1899 |
Missense Mutation |
GCG,GTG |
A552V |
XP_011526527.1 |
XM_011528226.2 |
1899 |
Missense Mutation |
GCG,GTG |
A552V |
XP_011526528.1 |
XM_011528227.2 |
1899 |
Missense Mutation |
GCG,GTG |
A502V |
XP_011526529.1 |
XM_017027177.1 |
1899 |
Intron |
|
|
XP_016882666.1 |
XM_017027178.1 |
1899 |
Missense Mutation |
GCG,GTG |
A582V |
XP_016882667.1 |
XM_017027179.1 |
1899 |
Missense Mutation |
GCG,GTG |
A581V |
XP_016882668.1 |
XM_017027180.1 |
1899 |
Intron |
|
|
XP_016882669.1 |
XM_017027181.1 |
1899 |
Intron |
|
|
XP_016882670.1 |
XM_017027182.1 |
1899 |
Missense Mutation |
GCG,GTG |
A553V |
XP_016882671.1 |
XM_017027183.1 |
1899 |
Intron |
|
|
XP_016882672.1 |
XM_017027184.1 |
1899 |
Intron |
|
|
XP_016882673.1 |
- Gene
- UQCR11
- Gene Name
- ubiquinol-cytochrome c reductase, complex III subunit XI
There are no transcripts associated with this gene.
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