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ACAGTAAATAAAATTATTTCTTTAA[C/T]TGTATTTTAAGGCAGCAGAACTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114204 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CACNA2D1 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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CACNA2D1 - calcium voltage-gated channel auxiliary subunit alpha2delta 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000722.3 | Intron | NP_000713.2 | ||||
NM_001302890.1 | Intron | NP_001289819.1 | ||||
XM_005250570.2 | Intron | XP_005250627.1 | ||||
XM_005250572.2 | Intron | XP_005250629.1 | ||||
XM_005250573.2 | Intron | XP_005250630.1 | ||||
XM_005250574.2 | Intron | XP_005250631.1 | ||||
XM_006716118.2 | Intron | XP_006716181.1 | ||||
XM_006716119.3 | Intron | XP_006716182.1 | ||||
XM_006716120.3 | Intron | XP_006716183.1 | ||||
XM_006716121.3 | Intron | XP_006716184.1 | ||||
XM_011516570.2 | Intron | XP_011514872.1 | ||||
XM_011516571.2 | Intron | XP_011514873.1 | ||||
XM_011516572.2 | Intron | XP_011514874.1 | ||||
XM_017012588.1 | Intron | XP_016868077.1 |