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CATAGAGGGTTAATCCATGTAAATT[A/G]GCTTCCACCCGTAAAGAAATTTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 613360 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DRAM2 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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DRAM2 - DNA damage regulated autophagy modulator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178454.4 | 1155 | Silent Mutation | GCC,GCT | A,A 239 | NP_848549.3 | |
XM_005270469.2 | 1155 | Silent Mutation | GCC,GCT | A,A 239 | XP_005270526.1 | |
XM_005270470.1 | 1155 | Silent Mutation | GCC,GCT | A,A 239 | XP_005270527.1 | |
XM_006710361.1 | 1155 | Silent Mutation | GCC,GCT | A,A 149 | XP_006710424.1 | |
XM_006710362.1 | 1155 | Silent Mutation | GCC,GCT | A,A 149 | XP_006710425.1 | |
XM_011540707.1 | 1155 | Silent Mutation | GCC,GCT | A,A 239 | XP_011539009.1 | |
XM_011540708.1 | 1155 | Silent Mutation | GCC,GCT | A,A 239 | XP_011539010.1 | |
XM_017000320.1 | 1155 | Silent Mutation | GCC,GCT | A,A 149 | XP_016855809.1 | |
XM_017000321.1 | 1155 | Silent Mutation | GCC,GCT | A,A 149 | XP_016855810.1 |