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TTTAAAAATAATATGTTCACATTGA[C/T]TTATAGTTCTTGTACTTAGTATCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 610044 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNT2 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
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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KCNT2 - potassium sodium-activated channel subfamily T member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287819.1 | Intron | NP_001274748.1 | ||||
NM_001287820.1 | Intron | NP_001274749.1 | ||||
NM_198503.3 | Intron | NP_940905.2 | ||||
XM_006711294.2 | Intron | XP_006711357.1 | ||||
XM_006711295.2 | Intron | XP_006711358.1 | ||||
XM_011509482.2 | Intron | XP_011507784.1 | ||||
XM_011509483.2 | Intron | XP_011507785.1 | ||||
XM_017001178.1 | Intron | XP_016856667.1 | ||||
XM_017001179.1 | Intron | XP_016856668.1 | ||||
XM_017001180.1 | Intron | XP_016856669.1 | ||||
XM_017001181.1 | Intron | XP_016856670.1 | ||||
XM_017001182.1 | Intron | XP_016856671.1 | ||||
XM_017001183.1 | Intron | XP_016856672.1 | ||||
XM_017001184.1 | Intron | XP_016856673.1 | ||||
XM_017001185.1 | Intron | XP_016856674.1 |