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- SNP ID:
- rs372592409
- Gene
-
DRAM2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 111120550 - 111120550 on Build GRCh38
- Polymorphism:
- C/A, Transversion substitution
- Context Sequence [VIC/FAM]:
CACTTACTCCACACCAGATAACCAA[C/A]AACAGTCTGATCCAGAAGACTTGTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 613360
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Literature Links: |
DRAM2 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 |
| DRAM2 - DNA damage regulated autophagy modulator 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_178454.4 | 921 | Missense Mutation | TTG,TTT | L,F 161 | NP_848549.3 | |
| XM_005270469.2 | 921 | Missense Mutation | TTG,TTT | L,F 161 | XP_005270526.1 | |
| XM_005270470.1 | 921 | Missense Mutation | TTG,TTT | L,F 161 | XP_005270527.1 | |
| XM_006710361.1 | 921 | Missense Mutation | TTG,TTT | L,F 71 | XP_006710424.1 | |
| XM_006710362.1 | 921 | Missense Mutation | TTG,TTT | L,F 71 | XP_006710425.1 | |
| XM_011540707.1 | 921 | Missense Mutation | TTG,TTT | L,F 161 | XP_011539009.1 | |
| XM_011540708.1 | 921 | Missense Mutation | TTG,TTT | L,F 161 | XP_011539010.1 | |
| XM_017000320.1 | 921 | Missense Mutation | TTG,TTT | L,F 71 | XP_016855809.1 | |
| XM_017000321.1 | 921 | Missense Mutation | TTG,TTT | L,F 71 | XP_016855810.1 | |
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