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TGTTTAGCTCTATTTCTTAGGGGCG[A/G]AAGCGTCCAGATAAGAATTTGTCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 182390 | ||||||||||||||||||||
Literature Links: |
SCN2A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SCN2A - sodium voltage-gated channel alpha subunit 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040142.1 | Intron | NP_001035232.1 | ||||
NM_001040143.1 | Intron | NP_001035233.1 | ||||
NM_021007.2 | Intron | NP_066287.2 | ||||
XM_005246753.3 | Intron | XP_005246810.1 | ||||
XM_005246755.4 | Intron | XP_005246812.1 | ||||
XM_017004655.1 | Intron | XP_016860144.1 | ||||
XM_017004656.1 | Intron | XP_016860145.1 | ||||
XM_017004657.1 | Intron | XP_016860146.1 | ||||
XM_017004658.1 | Intron | XP_016860147.1 | ||||
XM_017004659.1 | Intron | XP_016860148.1 |