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GGGGGGCCGCGGGCCGGCGGCGGGC[A/G]CACGGGCAGGGCAGGTCGGGGCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606898 MIM: 606900 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CACNG6 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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CACNG6 - calcium voltage-gated channel auxiliary subunit gamma 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031897.2 | 1289 | Silent Mutation | GCA,GCG | A,A 23 | NP_114103.2 | |
NM_145814.1 | 1289 | Silent Mutation | GCA,GCG | A,A 23 | NP_665813.1 | |
NM_145815.1 | 1289 | Silent Mutation | GCA,GCG | A,A 23 | NP_665814.1 | |
XM_006723316.3 | 1289 | Silent Mutation | GCA,GCG | A,A 23 | XP_006723379.1 |
CACNG8 - calcium voltage-gated channel auxiliary subunit gamma 8 | ||||||
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There are no transcripts associated with this gene. |