Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13240 | A10 | 14422582 | C | T | missense_variant | MODERATE | c.3844G>A|p.Val1282Ile |
S81 S85 |
2 | BAA10g13240 | A10 | 14422696 | C | T | missense_variant | MODERATE | c.3730G>A|p.Gly1244Ser |
S174 |
3 | BAA10g13240 | A10 | 14422700 | C | T | missense_variant | MODERATE | c.3726G>A|p.Met1242Ile |
S168 |
4 | BAA10g13240 | A10 | 14422788 | C | T | missense_variant | MODERATE | c.3638G>A|p.Arg1213Lys |
S238 |
5 | BAA10g13240 | A10 | 14423033 | C | T | synonymous_variant | LOW | c.3393G>A|p.Lys1131Lys |
S119 |
6 | BAA10g13240 | A10 | 14423044 | G | A | missense_variant | MODERATE | c.3382C>T|p.Arg1128Trp |
S278 |
7 | BAA10g13240 | A10 | 14423412 | C | T | missense_variant | MODERATE | c.3014G>A|p.Arg1005Lys |
S87 |
8 | BAA10g13240 | A10 | 14423829 | C | T | missense_variant | MODERATE | c.2668G>A|p.Ala890Thr |
S268 |
9 | BAA10g13240 | A10 | 14424988 | G | A | synonymous_variant | LOW | c.1509C>T|p.Leu503Leu |
S71 |
10 | BAA10g13240 | A10 | 14425608 | G | A | missense_variant | MODERATE | c.889C>T|p.Leu297Phe |
S71 |
11 | BAA10g13240 | A10 | 14425981 | G | A | synonymous_variant | LOW | c.516C>T|p.Asp172Asp |
S172 S217 |
12 | BAA10g13240 | A10 | 14426062 | C | T | synonymous_variant | LOW | c.435G>A|p.Arg145Arg |
S142 |
13 | BAA10g13240 | A10 | 14429862 | C | T | upstream_gene_variant | MODIFIER | c.-3366G>A| |
S79 S91 |
14 | BAA10g13240 | A10 | 14429922 | C | T | upstream_gene_variant | MODIFIER | c.-3426G>A| |
S23 |
15 | BAA10g13240 | A10 | 14430001 | C | A | upstream_gene_variant | MODIFIER | c.-3505G>T| |
S150 |
16 | BAA10g13240 | A10 | 14430180 | C | T | upstream_gene_variant | MODIFIER | c.-3684G>A| |
S191 |