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CAGTCTCAAAATTCATCTGGTAGCC[A/G]GCCAGCCAGCCCTCGTAACCTAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604492 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VDAC1 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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VDAC1 - voltage dependent anion channel 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003374.2 | 698 | Silent Mutation | GCC,GCT | A,A 151 | NP_003365.1 | |
XM_005272075.3 | 698 | Intron | XP_005272132.1 | |||
XM_017009821.1 | 698 | Intron | XP_016865310.1 | |||
XM_017009822.1 | 698 | Intron | XP_016865311.1 | |||
XM_017009823.1 | 698 | Intron | XP_016865312.1 |