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AATATGTTTTATTTCTGTAAGGTTA[A/G]TAATAATATTCCCTCTTTAATTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602106 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNJ15 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
|
KCNJ15 - potassium voltage-gated channel subfamily J member 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276435.1 | Intron | NP_001263364.1 | ||||
NM_001276436.1 | Intron | NP_001263365.1 | ||||
NM_001276437.1 | Intron | NP_001263366.1 | ||||
NM_001276438.1 | Intron | NP_001263367.1 | ||||
NM_001276439.1 | Intron | NP_001263368.1 | ||||
NM_002243.4 | Intron | NP_002234.2 | ||||
NM_170736.2 | Intron | NP_733932.1 | ||||
NM_170737.2 | Intron | NP_733933.1 | ||||
XM_005260975.2 | Intron | XP_005261032.1 | ||||
XM_006724002.2 | Intron | XP_006724065.1 | ||||
XM_011529560.2 | Intron | XP_011527862.1 | ||||
XM_011529561.2 | Intron | XP_011527863.1 | ||||
XM_017028343.1 | Intron | XP_016883832.1 | ||||
XM_017028344.1 | Intron | XP_016883833.1 | ||||
XM_017028345.1 | Intron | XP_016883834.1 |