| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 94801 | BAA10g03720 | A10 | 1785238 | G | A | upstream_gene_variant | MODIFIER | c.-2540G>A| |
S158 |
| 94802 | BAA10g03710 | A10 | 1785902 | G | A | missense_variant | MODERATE | c.1190C>T|p.Ala397Val |
S128 |
| 94803 | BAA10g03710 | A10 | 1786371 | C | T | missense_variant | MODERATE | c.721G>A|p.Asp241Asn |
S47 |
| 94804 | BAA10g03710 | A10 | 1787003 | G | A | missense_variant | MODERATE | c.233C>T|p.Pro78Leu |
S80 |
| 94805 | BAA10g03710 | A10 | 1787152 | G | A | synonymous_variant | LOW | c.84C>T|p.Leu28Leu |
S136 |
| 94806 | BAA10g03700 | A10 | 1787652 | C | T | upstream_gene_variant | MODIFIER | c.-2293G>A| |
S256 |
| 94807 | BAA10g03720 | A10 | 1787798 | C | T | synonymous_variant | LOW | c.21C>T|p.Cys7Cys |
S47 |
| 94808 | BAA10g03720 | A10 | 1787885 | C | T | synonymous_variant | LOW | c.108C>T|p.Asn36Asn |
S193 |
| 94809 | BAA10g03700 | A10 | 1788390 | G | A | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S158 |
| 94810 | BAA10g03720 | A10 | 1788788 | G | A | missense_variant | MODERATE | c.685G>A|p.Ala229Thr |
S303 |
| 94811 | BAA10g03720 | A10 | 1788834 | C | T | missense_variant | MODERATE | c.731C>T|p.Ser244Phe |
S68 |
| 94812 | BAA10g03720 | A10 | 1789273 | G | A | synonymous_variant | LOW | c.1092G>A|p.Ala364Ala |
S191 |
| 94813 | BAA10g03720 | A10 | 1789424 | G | A | missense_variant | MODERATE | c.1163G>A|p.Gly388Glu |
S236 |
| 94814 | BAA10g03720 | A10 | 1789639 | G | A | synonymous_variant | LOW | c.1287G>A|p.Val429Val |
S168 |
| 94815 | BAA10g03700 | A10 | 1790160 | G | A | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S18 |
| 94816 | BAA10g03730 | A10 | 1795649 | G | A | missense_variant | MODERATE | c.401G>A|p.Gly134Asp |
S217 S248 |
| 94817 | BAA10g03730 | A10 | 1796158 | C | T | downstream_gene_variant | MODIFIER | c.*65C>T| |
S181 |
| 94818 | BAA10g03730 | A10 | 1798857 | C | T | downstream_gene_variant | MODIFIER | c.*2764C>T| |
S195 |
| 94819 | BAA10g03730 | A10 | 1799989 | G | A | downstream_gene_variant | MODIFIER | c.*3896G>A| |
S267 |
| 94820 | BAA10g03750 | A10 | 1801407 | C | T | downstream_gene_variant | MODIFIER | c.*1246G>A| |
S197 |
| 94821 | BAA10g03740 | A10 | 1801777 | C | T | stop_gained | HIGH | c.173G>A|p.Trp58* |
S233 |
| 94822 | BAA10g03740 | A10 | 1801891 | G | A | splice_region_variant&intron_variant | LOW | c.126+3C>T| |
S179 |
| 94823 | BAA10g03750 | A10 | 1802813 | G | A | missense_variant | MODERATE | c.1061C>T|p.Pro354Leu |
S216 |
| 94824 | BAA10g03750 | A10 | 1804376 | G | A | missense_variant | MODERATE | c.205C>T|p.Arg69Cys |
S20 |
| 94825 | BAA10g03750 | A10 | 1804400 | G | A | missense_variant | MODERATE | c.181C>T|p.Leu61Phe |
S18 |