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TCTCCTTTATGGGAGATCTTTGCTT[G/T]GAATACATCCGTTGGTAGGGAACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600702 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SCN8A 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) - 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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SCN8A - sodium voltage-gated channel alpha subunit 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177984.2 | Intron | NP_001171455.1 | ||||
NM_014191.3 | Intron | NP_055006.1 | ||||
XM_006719556.3 | Intron | XP_006719619.1 | ||||
XM_011538650.2 | Intron | XP_011536952.1 | ||||
XM_011538651.2 | Intron | XP_011536953.1 | ||||
XM_017019794.1 | Intron | XP_016875283.1 | ||||
XM_017019795.1 | Intron | XP_016875284.1 | ||||
XM_017019796.1 | Intron | XP_016875285.1 |