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- SNP ID:
- rs10423327
- Gene
-
STK11 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.19: 1214409 - 1214409 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GCTCAGGAGTGCCTGGGCTCTTCCA[C/T]GTTTCAGCTGCTGTGTGTCCTGCTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602216
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Literature Links: |
STK11 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
|
| STK11 - serine/threonine kinase 11 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000455.4 | Intron | NP_000446.1 | ||||
| XM_005259617.2 | Intron | XP_005259674.1 | ||||
| XM_005259618.3 | Intron | XP_005259675.1 | ||||
| XM_011528209.1 | Intron | XP_011526511.1 | ||||
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