Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07200 | A10 | 4012074 | G | A | missense_variant | MODERATE | c.623G>A|p.Gly208Glu |
S69 |
2 | BAA10g07200 | A10 | 4012116 | G | A | missense_variant | MODERATE | c.665G>A|p.Gly222Glu |
S120 |
3 | BAA10g07200 | A10 | 4012262 | G | A | missense_variant | MODERATE | c.811G>A|p.Ala271Thr |
S164 |
4 | BAA10g07200 | A10 | 4012827 | G | A | missense_variant | MODERATE | c.1376G>A|p.Gly459Glu |
S125 |
5 | BAA10g07200 | A10 | 4014923 | G | A | downstream_gene_variant | MODIFIER | c.*47G>A| |
S53 |
6 | BAA10g07200 | A10 | 4015118 | C | T | downstream_gene_variant | MODIFIER | c.*242C>T| |
S260 |
7 | BAA10g07200 | A10 | 4016069 | G | A | downstream_gene_variant | MODIFIER | c.*1193G>A| |
S252 |
8 | BAA10g07200 | A10 | 4016126 | C | T | downstream_gene_variant | MODIFIER | c.*1250C>T| |
S40 S49 |
9 | BAA10g07200 | A10 | 4016817 | G | A | downstream_gene_variant | MODIFIER | c.*1941G>A| |
S120 |