Product Details
- SNP ID
-
rs141593934
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:89738067 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGACTATTCACATGAAACTGCGTCC[A/G]CCGACGATGCTGGAATCCAATATTC
- Phenotype
-
MIM: 608689
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MESP1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs35017767] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- MESP1
- Gene Name
- mesoderm posterior bHLH transcription factor 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_018670.3 |
1815 |
Intron |
|
|
NP_061140.1 |
- Gene
- WDR93
- Gene Name
- WD repeat domain 93
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001284395.1 |
1815 |
Missense Mutation |
ACC,GCC |
T570A |
NP_001271324.1 |
NM_001284396.1 |
1815 |
Intron |
|
|
NP_001271325.1 |
NM_020212.1 |
1815 |
Missense Mutation |
ACC,GCC |
T598A |
NP_064597.1 |
XM_006720614.1 |
1815 |
Silent Mutation |
CCA,CCG |
P576P |
XP_006720677.1 |
XM_006720615.1 |
1815 |
Silent Mutation |
CCA,CCG |
P547P |
XP_006720678.1 |
XM_006720618.2 |
1815 |
Intron |
|
|
XP_006720681.1 |
XM_011521794.2 |
1815 |
Silent Mutation |
CCA,CCG |
P576P |
XP_011520096.1 |
XM_011521795.1 |
1815 |
Silent Mutation |
CCA,CCG |
P576P |
XP_011520097.1 |
XM_011521796.2 |
1815 |
Intron |
|
|
XP_011520098.1 |
XM_011521798.2 |
1815 |
Silent Mutation |
CCA,CCG |
P378P |
XP_011520100.1 |
XM_011521800.1 |
1815 |
Silent Mutation |
CCA,CCG |
P378P |
XP_011520102.1 |
XM_011521802.2 |
1815 |
Intron |
|
|
XP_011520104.1 |
XM_017022415.1 |
1815 |
Silent Mutation |
CCA,CCG |
P400P |
XP_016877904.1 |
XM_017022416.1 |
1815 |
Silent Mutation |
CCA,CCG |
P378P |
XP_016877905.1 |
XM_017022417.1 |
1815 |
Intron |
|
|
XP_016877906.1 |
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