Product Details
- SNP ID
-
rs35017767
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:89738150 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCTGGAAAATATCTCAAAAAATTG[C/T]ACCATTCCTCAAAGGGACTTGGATA
- Phenotype
-
MIM: 608689
- Polymorphism
- C/T, Transition 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 |
1898 |
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 |
1898 |
Silent Mutation |
TGC,TGT |
C597C |
NP_001271324.1 |
| NM_001284396.1 |
1898 |
Intron |
|
|
NP_001271325.1 |
| NM_020212.1 |
1898 |
Silent Mutation |
TGC,TGT |
C625C |
NP_064597.1 |
| XM_006720614.1 |
1898 |
Missense Mutation |
GCA,GTA |
A604V |
XP_006720677.1 |
| XM_006720615.1 |
1898 |
Missense Mutation |
GCA,GTA |
A575V |
XP_006720678.1 |
| XM_006720618.2 |
1898 |
Intron |
|
|
XP_006720681.1 |
| XM_011521794.2 |
1898 |
Missense Mutation |
GCA,GTA |
A604V |
XP_011520096.1 |
| XM_011521795.1 |
1898 |
Missense Mutation |
GCA,GTA |
A604V |
XP_011520097.1 |
| XM_011521796.2 |
1898 |
Nonsense Mutation |
TGC,TGT |
C579C |
XP_011520098.1 |
| XM_011521798.2 |
1898 |
Missense Mutation |
GCA,GTA |
A406V |
XP_011520100.1 |
| XM_011521800.1 |
1898 |
Missense Mutation |
GCA,GTA |
A406V |
XP_011520102.1 |
| XM_011521802.2 |
1898 |
Intron |
|
|
XP_011520104.1 |
| XM_017022415.1 |
1898 |
Missense Mutation |
GCA,GTA |
A428V |
XP_016877904.1 |
| XM_017022416.1 |
1898 |
Missense Mutation |
GCA,GTA |
A406V |
XP_016877905.1 |
| XM_017022417.1 |
1898 |
Intron |
|
|
XP_016877906.1 |
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