Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08740 | A10 | 10704321 | G | A | synonymous_variant | LOW | c.1381C>T|p.Leu461Leu |
S208 S219 |
2 | BAA10g08740 | A10 | 10704781 | C | T | missense_variant | MODERATE | c.1069G>A|p.Glu357Lys |
S119 |
3 | BAA10g08740 | A10 | 10705363 | G | A | missense_variant | MODERATE | c.886C>T|p.Pro296Ser |
S257 |
4 | BAA10g08740 | A10 | 10705653 | G | A | synonymous_variant | LOW | c.739C>T|p.Leu247Leu |
S198 |
5 | BAA10g08740 | A10 | 10706475 | G | A | stop_gained | HIGH | c.304C>T|p.Gln102* |
S192 |
6 | BAA10g08740 | A10 | 10706562 | C | T | missense_variant | MODERATE | c.217G>A|p.Ala73Thr |
S156 |
7 | BAA10g08740 | A10 | 10707205 | G | A | upstream_gene_variant | MODIFIER | c.-203C>T| |
S13 |
8 | BAA10g08740 | A10 | 10707700 | G | A | upstream_gene_variant | MODIFIER | c.-698C>T| |
S165 |
9 | BAA10g08740 | A10 | 10707842 | G | A | upstream_gene_variant | MODIFIER | c.-840C>T| |
S184 |
10 | BAA10g08740 | A10 | 10708759 | C | T | upstream_gene_variant | MODIFIER | c.-1757G>A| |
S305 |
11 | BAA10g08740 | A10 | 10709066 | G | A | upstream_gene_variant | MODIFIER | c.-2064C>T| |
S216 |
12 | BAA10g08740 | A10 | 10709086 | C | T | upstream_gene_variant | MODIFIER | c.-2084G>A| |
S146 |
13 | BAA10g08740 | A10 | 10709395 | C | T | upstream_gene_variant | MODIFIER | c.-2393G>A| |
S238 |