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- SNP ID:
- rs777237633
- Gene
-
MAPK9 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.5: 180265913 - 180265913 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
AAATCTAAAACATGAAATAAAACCT[C/G]AGAATATAGATAAACATTTATATAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602896
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Literature Links: |
MAPK9 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| MAPK9 - mitogen-activated protein kinase 9 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001135044.1 | Intron | NP_001128516.1 | ||||
| NM_001308244.1 | Intron | NP_001295173.1 | ||||
| NM_002752.4 | Intron | NP_002743.3 | ||||
| NM_139068.2 | Intron | NP_620707.1 | ||||
| NM_139069.2 | Intron | NP_620708.1 | ||||
| NM_139070.2 | Intron | NP_620709.1 | ||||
| XM_005265940.4 | Intron | XP_005265997.1 | ||||
| XM_006714891.2 | Intron | XP_006714954.1 | ||||
| XM_017009638.1 | Intron | XP_016865127.1 | ||||
| XM_017009639.1 | Intron | XP_016865128.1 | ||||
| XM_017009640.1 | Intron | XP_016865129.1 | ||||
| XM_017009641.1 | Intron | XP_016865130.1 | ||||
| XM_017009642.1 | Intron | XP_016865131.1 | ||||
| XM_017009643.1 | Intron | XP_016865132.1 | ||||
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