| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 113651 | BAA10g08960 | A10 | 11013764 | G | A | missense_variant | MODERATE | c.271G>A|p.Gly91Ser |
S57 |
| 113652 | BAA10g08960 | A10 | 11014105 | C | T | synonymous_variant | LOW | c.612C>T|p.Asp204Asp |
S176 |
| 113653 | BAA10g08960 | A10 | 11014446 | G | A | missense_variant | MODERATE | c.929G>A|p.Gly310Glu |
S192 |
| 113654 | BAA10g08960 | A10 | 11014488 | G | A | missense_variant | MODERATE | c.971G>A|p.Arg324Lys |
S140 |
| 113655 | BAA10g08960 | A10 | 11014672 | G | A | intron_variant | MODIFIER | c.1144+11G>A| |
S251 |
| 113656 | BAA10g08960 | A10 | 11014689 | G | A | intron_variant | MODIFIER | c.1144+28G>A| |
S138 |
| 113657 | BAA10g08960 | A10 | 11016380 | G | A | downstream_gene_variant | MODIFIER | c.*1583G>A| |
S107 |
| 113658 | BAA10g08960 | A10 | 11019412 | C | T | downstream_gene_variant | MODIFIER | c.*4615C>T| |
S166 |
| 113659 | BAA10g08970 | A10 | 11020287 | G | A | downstream_gene_variant | MODIFIER | c.*4114C>T| |
S236 |
| 113660 | BAA10g08970 | A10 | 11020594 | G | A | downstream_gene_variant | MODIFIER | c.*3807C>T| |
S172 S217 |
| 113661 | BAA10g08970 | A10 | 11020876 | C | T | downstream_gene_variant | MODIFIER | c.*3525G>A| |
S237 |
| 113662 | BAA10g08970 | A10 | 11021186 | C | T | downstream_gene_variant | MODIFIER | c.*3215G>A| |
S155 S211 |
| 113663 | BAA10g08970 | A10 | 11021444 | C | T | downstream_gene_variant | MODIFIER | c.*2957G>A| |
S203 |
| 113664 | BAA10g08970 | A10 | 11021547 | G | A | downstream_gene_variant | MODIFIER | c.*2854C>T| |
S192 |
| 113665 | BAA10g08970 | A10 | 11022224 | C | T | downstream_gene_variant | MODIFIER | c.*2177G>A| |
S156 |
| 113666 | BAA10g08970 | A10 | 11022361 | C | T | downstream_gene_variant | MODIFIER | c.*2040G>A| |
S244 |
| 113667 | BAA10g08970 | A10 | 11024356 | C | T | downstream_gene_variant | MODIFIER | c.*45G>A| |
S2 |
| 113668 | BAA10g08970 | A10 | 11024586 | C | T | missense_variant | MODERATE | c.1279G>A|p.Val427Met |
S117 |
| 113669 | BAA10g08970 | A10 | 11025551 | C | T | missense_variant | MODERATE | c.347G>A|p.Arg116Lys |
S97 |
| 113670 | BAA10g08970 | A10 | 11025561 | C | T | missense_variant | MODERATE | c.337G>A|p.Asp113Asn |
S146 |
| 113671 | BAA10g08970 | A10 | 11025691 | C | T | synonymous_variant | LOW | c.207G>A|p.Arg69Arg |
S10 |
| 113672 | BAA10g08970 | A10 | 11026907 | C | T | upstream_gene_variant | MODIFIER | c.-1010G>A| |
S179 |
| 113673 | BAA10g08970 | A10 | 11026925 | C | T | upstream_gene_variant | MODIFIER | c.-1028G>A| |
S249 |
| 113674 | BAA10g08970 | A10 | 11027013 | C | T | upstream_gene_variant | MODIFIER | c.-1116G>A| |
S56 |
| 113675 | BAA10g08970 | A10 | 11027521 | G | A | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S295 |