Product Details
- SNP ID
-
rs199697478
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:36583676 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTGCCATATCCTTACTGGAGAGAT[C/G]GTAGCTATAAAAATCATGGATAAAA
- Phenotype
-
MIM: 607025
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MELK
PubMed Links
Gene Details
- Gene
- MELK
- Gene Name
- maternal embryonic leucine zipper kinase
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001256685.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
NP_001243614.1 |
| NM_001256687.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
NP_001243616.1 |
| NM_001256688.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
NP_001243617.1 |
| NM_001256689.1 |
292 |
Intron |
|
|
NP_001243618.1 |
| NM_001256690.1 |
292 |
Intron |
|
|
NP_001243619.1 |
| NM_001256691.1 |
292 |
Intron |
|
|
NP_001243620.1 |
| NM_001256692.1 |
292 |
Intron |
|
|
NP_001243621.1 |
| NM_001256693.1 |
292 |
Intron |
|
|
NP_001243622.1 |
| NM_014791.3 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
NP_055606.1 |
| XM_011518076.2 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516378.1 |
| XM_011518077.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516379.1 |
| XM_011518078.2 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516380.1 |
| XM_011518079.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516381.1 |
| XM_011518080.1 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516382.1 |
| XM_011518081.2 |
292 |
Intron |
|
|
XP_011516383.1 |
| XM_011518082.2 |
292 |
Intron |
|
|
XP_011516384.1 |
| XM_011518083.2 |
292 |
Intron |
|
|
XP_011516385.1 |
| XM_011518084.2 |
292 |
Intron |
|
|
XP_011516386.1 |
| XM_011518085.1 |
292 |
Intron |
|
|
XP_011516387.1 |
| XM_011518086.2 |
292 |
Missense Mutation |
ATC,ATG |
I36M |
XP_011516388.1 |
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