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CAGACCGAGAGTGTGACCAGAGGCC[A/C]TGAGAGCCCCGGACACAGGCAGGGC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602906 MIM: 605030 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNS2 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
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
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KCNS2 - potassium voltage-gated channel modifier subfamily S member 2 | ||||||
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There are no transcripts associated with this gene. |
STK3 - serine/threonine kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256312.1 | Intron | NP_001243241.1 | ||||
NM_001256313.1 | Intron | NP_001243242.1 | ||||
NM_006281.3 | Intron | NP_006272.2 | ||||
XM_011517248.2 | Intron | XP_011515550.2 | ||||
XM_011517251.1 | Intron | XP_011515553.1 | ||||
XM_011517252.2 | Intron | XP_011515554.2 | ||||
XM_011517253.2 | Intron | XP_011515555.1 | ||||
XM_011517255.2 | Intron | XP_011515557.1 | ||||
XM_011517257.2 | Intron | XP_011515559.2 | ||||
XM_011517258.1 | Intron | XP_011515560.1 | ||||
XM_017013756.1 | Intron | XP_016869245.1 | ||||
XM_017013757.1 | Intron | XP_016869246.1 | ||||
XM_017013758.1 | Intron | XP_016869247.1 | ||||
XM_017013759.1 | Intron | XP_016869248.1 | ||||
XM_017013760.1 | Intron | XP_016869249.1 | ||||
XM_017013761.1 | Intron | XP_016869250.1 | ||||
XM_017013762.1 | Intron | XP_016869251.1 | ||||
XM_017013763.1 | Intron | XP_016869252.1 | ||||
XM_017013764.1 | Intron | XP_016869253.1 | ||||
XM_017013765.1 | Intron | XP_016869254.1 |
Set Membership: |
HapMap |