Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08170 | A08 | 7495142 | C | T | missense_variant | MODERATE | c.1786G>A|p.Glu596Lys |
S151 S153 S157 S167 S236 S262 S263 |
2 | BAA08g08170 | A08 | 7495363 | C | T | missense_variant | MODERATE | c.1565G>A|p.Gly522Glu |
S291 |
3 | BAA08g08170 | A08 | 7495715 | G | A | missense_variant | MODERATE | c.1213C>T|p.Leu405Phe |
S241 |
4 | BAA08g08170 | A08 | 7495726 | G | A | missense_variant | MODERATE | c.1202C>T|p.Thr401Ile |
S199 |
5 | BAA08g08170 | A08 | 7496045 | G | A | stop_gained | HIGH | c.883C>T|p.Gln295* |
S246 |
6 | BAA08g08170 | A08 | 7496441 | C | T | missense_variant | MODERATE | c.487G>A|p.Asp163Asn |
S155 S211 |
7 | BAA08g08170 | A08 | 7496593 | G | A | missense_variant | MODERATE | c.335C>T|p.Ala112Val |
S186 |
8 | BAA08g08170 | A08 | 7496772 | C | T | missense_variant | MODERATE | c.156G>A|p.Met52Ile |
S169 |
9 | BAA08g08170 | A08 | 7496833 | C | T | missense_variant | MODERATE | c.95G>A|p.Cys32Tyr |
S177 |
10 | BAA08g08170 | A08 | 7497027 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S287 |
11 | BAA08g08170 | A08 | 7497082 | C | T | upstream_gene_variant | MODIFIER | c.-155G>A| |
S276 |
12 | BAA08g08170 | A08 | 7498213 | C | T | upstream_gene_variant | MODIFIER | c.-1286G>A| |
S215 |
13 | BAA08g08170 | A08 | 7498412 | G | A | upstream_gene_variant | MODIFIER | c.-1485C>T| |
S13 |
14 | BAA08g08170 | A08 | 7500148 | C | T | upstream_gene_variant | MODIFIER | c.-3221G>A| |
S71 |
15 | BAA08g08170 | A08 | 7500644 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S156 |
16 | BAA08g08170 | A08 | 7501452 | G | A | upstream_gene_variant | MODIFIER | c.-4525C>T| |
S10 |
17 | BAA08g08170 | A08 | 7501472 | C | T | upstream_gene_variant | MODIFIER | c.-4545G>A| |
S12 |