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AGAATACTGTTGTGGTCTTAGAAAT[A/G]TGAATAAAACTCATCAAAAGTATAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
|
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Phenotype: |
MIM: 603219 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNK2 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
|
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AMR
|
KCNK2 - potassium two pore domain channel subfamily K member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017424.2 | Intron | NP_001017424.1 | ||||
NM_001017425.2 | Intron | NP_001017425.2 | ||||
NM_014217.3 | Intron | NP_055032.1 | ||||
XM_011509522.2 | Intron | XP_011507824.1 | ||||
XM_011509523.1 | Intron | XP_011507825.1 | ||||
XM_011509524.2 | Intron | XP_011507826.1 | ||||
XM_017001248.1 | Intron | XP_016856737.1 | ||||
XM_017001249.1 | Intron | XP_016856738.1 |