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- SNP ID:
- rs566593066
- Gene
-
MAP4K2MEN1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 64805655 - 64805655 on Build GRCh38
- Polymorphism:
- G/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TTCACCTGGCTTTGCTCCCCCGGCC[G/C]CTCCTCGCCCGCCTCCAGCAAGCTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603166
MIM: 613733
|
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Literature Links: |
MAP4K2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| MAP4K2 - mitogen-activated protein kinase kinase kinase kinase 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MEN1 - menin 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000244.3 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_000235.2 | |
| NM_130799.2 | 1657 | Missense Mutation | CGG,GGG | R,G 389 | NP_570711.1 | |
| NM_130800.2 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_570712.1 | |
| NM_130801.2 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_570713.1 | |
| NM_130802.2 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_570714.1 | |
| NM_130803.2 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_570715.1 | |
| NM_130804.2 | 1657 | Missense Mutation | CGG,GGG | R,G 394 | NP_570716.1 | |
| XM_005274001.4 | 1657 | Missense Mutation | CGG,GGG | R,G 389 | XP_005274058.1 | |
| XM_011545040.1 | 1657 | Missense Mutation | CGG,GGG | R,G 431 | XP_011543342.1 | |
| XM_011545041.2 | 1657 | Missense Mutation | CGG,GGG | R,G 431 | XP_011543343.1 | |
| XM_011545042.2 | 1657 | Missense Mutation | CGG,GGG | R,G 431 | XP_011543344.1 | |
| XM_017017765.1 | 1657 | Missense Mutation | CGG,GGG | R,G 436 | XP_016873254.1 | |
| XM_017017766.1 | 1657 | Missense Mutation | CGG,GGG | R,G 436 | XP_016873255.1 | |
| XM_017017767.1 | 1657 | Missense Mutation | CGG,GGG | R,G 436 | XP_016873256.1 | |
| XM_017017768.1 | 1657 | Missense Mutation | CGG,GGG | R,G 436 | XP_016873257.1 | |
| XM_017017769.1 | 1657 | Missense Mutation | CGG,GGG | R,G 389 | XP_016873258.1 | |
| XM_017017770.1 | 1657 | Missense Mutation | CGG,GGG | R,G 389 | XP_016873259.1 | |
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