Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCTGAGGTTTTCCACCCCGAGGAC[C/T]CTTGTCTGCGGATCCACCACGGCAG
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 - 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 |
CACNA1D - calcium voltage-gated channel subunit alpha1 D | ||||||
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There are no transcripts associated with this gene. |
CHDH - choline dehydrogenase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018397.4 | 1822 | Silent Mutation | NP_060867.2 | |||
XM_006713250.3 | 1822 | Missense Mutation | XP_006713313.1 | |||
XM_006713251.3 | 1822 | Missense Mutation | XP_006713314.1 | |||
XM_006713252.3 | 1822 | UTR 3 | XP_006713315.1 | |||
XM_011533938.2 | 1822 | Missense Mutation | XP_011532240.1 | |||
XM_011533939.2 | 1822 | Missense Mutation | XP_011532241.1 | |||
XM_017006797.1 | 1822 | Missense Mutation | XP_016862286.1 | |||
XM_017006798.1 | 1822 | Missense Mutation | XP_016862287.1 | |||
XM_017006799.1 | 1822 | UTR 3 | XP_016862288.1 |