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CCCAAAGAAGAAAAACAATCATTTT[A/G]GCAGATGTCAAATTTTGTGTTGCCA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 114206 | |||||||||||||||||||||||
Literature Links: |
CACNA1D PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CACNA1D - calcium voltage-gated channel subunit alpha1 D | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000720.3 | 296 | Intron | NP_000711.1 | |||
NM_001128839.2 | 296 | Intron | NP_001122311.1 | |||
NM_001128840.2 | 296 | Intron | NP_001122312.1 | |||
XM_005265448.3 | 296 | Intron | XP_005265505.1 | |||
XM_011534094.2 | 296 | Intron | XP_011532396.1 | |||
XM_011534096.2 | 296 | Intron | XP_011532398.1 | |||
XM_011534097.2 | 296 | UTR 5 | XP_011532399.1 | |||
XM_011534099.2 | 296 | Intron | XP_011532401.1 | |||
XM_011534100.2 | 296 | Intron | XP_011532402.1 | |||
XM_017007137.1 | 296 | Intron | XP_016862626.1 | |||
XM_017007138.1 | 296 | Intron | XP_016862627.1 | |||
XM_017007139.1 | 296 | Intron | XP_016862628.1 | |||
XM_017007140.1 | 296 | Intron | XP_016862629.1 | |||
XM_017007141.1 | 296 | Intron | XP_016862630.1 | |||
XM_017007142.1 | 296 | Intron | XP_016862631.1 | |||
XM_017007143.1 | 296 | Intron | XP_016862632.1 | |||
XM_017007144.1 | 296 | Intron | XP_016862633.1 | |||
XM_017007145.1 | 296 | Intron | XP_016862634.1 |