Product Details
- SNP ID
-
rs148853182
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:89737620 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTCTGTGTGCCTTATGGATGTGGC[A/C]AAGCGTGAAATCATCTGTGCCTTTG
- Phenotype
-
MIM: 608689
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
MESP1
PubMed Links
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 |
1679 |
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 |
1679 |
Silent Mutation |
GCA,GCC |
A524A |
NP_001271324.1 |
NM_001284396.1 |
1679 |
Intron |
|
|
NP_001271325.1 |
NM_020212.1 |
1679 |
Silent Mutation |
GCA,GCC |
A552A |
NP_064597.1 |
XM_006720614.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q531P |
XP_006720677.1 |
XM_006720615.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q502P |
XP_006720678.1 |
XM_006720618.2 |
1679 |
Intron |
|
|
XP_006720681.1 |
XM_011521794.2 |
1679 |
Missense Mutation |
CAA,CCA |
Q531P |
XP_011520096.1 |
XM_011521795.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q531P |
XP_011520097.1 |
XM_011521796.2 |
1679 |
Missense Mutation |
CAA,CCA |
Q531P |
XP_011520098.1 |
XM_011521798.2 |
1679 |
Missense Mutation |
CAA,CCA |
Q333P |
XP_011520100.1 |
XM_011521800.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q333P |
XP_011520102.1 |
XM_011521802.2 |
1679 |
Intron |
|
|
XP_011520104.1 |
XM_017022415.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q355P |
XP_016877904.1 |
XM_017022416.1 |
1679 |
Missense Mutation |
CAA,CCA |
Q333P |
XP_016877905.1 |
XM_017022417.1 |
1679 |
Intron |
|
|
XP_016877906.1 |
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