Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08290 | A08 | 7577759 | G | A | missense_variant | MODERATE | c.65G>A|p.Arg22Lys |
S260 |
2 | BAA08g08290 | A08 | 7578167 | C | T | stop_gained | HIGH | c.385C>T|p.Gln129* |
S140 |
3 | BAA08g08290 | A08 | 7578205 | G | A | missense_variant | MODERATE | c.423G>A|p.Met141Ile |
S281 |
4 | BAA08g08290 | A08 | 7579106 | C | T | intron_variant | MODIFIER | c.773+461C>T| |
S305 |
5 | BAA08g08290 | A08 | 7580515 | G | A | intron_variant | MODIFIER | c.1011+68G>A| |
S159 |
6 | BAA08g08290 | A08 | 7580917 | C | T | intron_variant | MODIFIER | c.1012-212C>T| |
S83 S88 |
7 | BAA08g08290 | A08 | 7581439 | C | T | missense_variant | MODERATE | c.1322C>T|p.Ser441Leu |
S276 |
8 | BAA08g08290 | A08 | 7582197 | C | T | missense_variant | MODERATE | c.2080C>T|p.Leu694Phe |
S281 |
9 | BAA08g08290 | A08 | 7582928 | T | C | intron_variant | MODIFIER | c.2588+135T>C| |
S134 |
10 | BAA08g08290 | A08 | 7583330 | G | A | intron_variant | MODIFIER | c.2588+537G>A| |
S260 |
11 | BAA08g08290 | A08 | 7583867 | A | T | intron_variant | MODIFIER | c.2589-840A>T| |
S286 |
12 | BAA08g08290 | A08 | 7583935 | G | A | intron_variant | MODIFIER | c.2589-772G>A| |
S148 S210 |
13 | BAA08g08290 | A08 | 7586069 | G | A | downstream_gene_variant | MODIFIER | c.*904G>A| |
S306 S308 |
14 | BAA08g08290 | A08 | 7586351 | G | A | downstream_gene_variant | MODIFIER | c.*1186G>A| |
S241 |
15 | BAA08g08290 | A08 | 7587260 | G | A | downstream_gene_variant | MODIFIER | c.*2095G>A| |
S240 |
16 | BAA08g08290 | A08 | 7588434 | C | T | downstream_gene_variant | MODIFIER | c.*3269C>T| |
S143 |
17 | BAA08g08290 | A08 | 7589565 | C | T | downstream_gene_variant | MODIFIER | c.*4400C>T| |
S208 S93 |
18 | BAA08g08290 | A08 | 7590091 | C | T | downstream_gene_variant | MODIFIER | c.*4926C>T| |
S178 |