| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 124601 | BAA10g14080 | A10 | 14947811 | C | T | upstream_gene_variant | MODIFIER | c.-3610G>A| |
S187 |
| 124602 | BAA10g14090 | A10 | 14948648 | G | A | missense_variant | MODERATE | c.557G>A|p.Gly186Glu |
S71 |
| 124603 | BAA10g14090 | A10 | 14949240 | G | A | downstream_gene_variant | MODIFIER | c.*90G>A| |
S55 |
| 124604 | BAA10g14090 | A10 | 14949688 | G | A | downstream_gene_variant | MODIFIER | c.*538G>A| |
S72 S78 |
| 124605 | BAA10g14100 | A10 | 14950340 | G | A | missense_variant | MODERATE | c.1081C>T|p.Pro361Ser |
S279 |
| 124606 | BAA10g14100 | A10 | 14951235 | G | A | missense_variant | MODERATE | c.262C>T|p.Pro88Ser |
S127 |
| 124607 | BAA10g14090 | A10 | 14952147 | G | A | downstream_gene_variant | MODIFIER | c.*2997G>A| |
S40 S49 |
| 124608 | BAA10g14100 | A10 | 14952598 | C | T | upstream_gene_variant | MODIFIER | c.-209G>A| |
S28 |
| 124609 | BAA10g14100 | A10 | 14952600 | G | C | upstream_gene_variant | MODIFIER | c.-211C>G| |
S28 |
| 124610 | BAA10g14100 | A10 | 14953123 | C | T | upstream_gene_variant | MODIFIER | c.-734G>A| |
S113 |
| 124611 | BAA10g14110 | A10 | 14954644 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1328-1G>A| |
S177 |
| 124612 | BAA10g14110 | A10 | 14954964 | G | A | missense_variant | MODERATE | c.1088C>T|p.Thr363Met |
S239 |
| 124613 | BAA10g14110 | A10 | 14955005 | C | T | synonymous_variant | LOW | c.1047G>A|p.Gly349Gly |
S42 |
| 124614 | BAA10g14110 | A10 | 14955230 | C | T | missense_variant | MODERATE | c.973G>A|p.Glu325Lys |
S260 |
| 124615 | BAA10g14110 | A10 | 14955290 | G | A | missense_variant | MODERATE | c.913C>T|p.Pro305Ser |
S34 |
| 124616 | BAA10g14100 | A10 | 14955506 | G | A | upstream_gene_variant | MODIFIER | c.-3117C>T| |
S219 S72 |
| 124617 | BAA10g14110 | A10 | 14955694 | C | T | missense_variant | MODERATE | c.788G>A|p.Gly263Asp |
S60 |
| 124618 | BAA10g14110 | A10 | 14955848 | C | T | missense_variant | MODERATE | c.634G>A|p.Glu212Lys |
S121 |
| 124619 | BAA10g14100 | A10 | 14956261 | C | T | upstream_gene_variant | MODIFIER | c.-3872G>A| |
S200 |
| 124620 | BAA10g14110 | A10 | 14958255 | C | T | upstream_gene_variant | MODIFIER | c.-995G>A| |
S44 |
| 124621 | BAA10g14110 | A10 | 14959084 | G | A | upstream_gene_variant | MODIFIER | c.-1824C>T| |
S257 |
| 124622 | BAA10g14110 | A10 | 14959428 | G | A | upstream_gene_variant | MODIFIER | c.-2168C>T| |
S17 |
| 124623 | BAA10g14130 | A10 | 14961452 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S113 |
| 124624 | BAA10g14130 | A10 | 14961714 | G | A | missense_variant | MODERATE | c.170G>A|p.Arg57Lys |
S245 |
| 124625 | BAA10g14140 | A10 | 14965429 | G | A | synonymous_variant | LOW | c.1780C>T|p.Leu594Leu |
S111 |