| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 147901 | BAA10g32300 | A10 | 23270856 | G | A | upstream_gene_variant | MODIFIER | c.-900C>T| |
S106 |
| 147902 | BAA10g32300 | A10 | 23271245 | G | A | upstream_gene_variant | MODIFIER | c.-1289C>T| |
S286 |
| 147903 | BAA10g32300 | A10 | 23273297 | G | A | upstream_gene_variant | MODIFIER | c.-3341C>T| |
S223 |
| 147904 | BAA10g32320 | A10 | 23274398 | C | T | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S187 |
| 147905 | BAA10g32310 | A10 | 23275174 | C | T | downstream_gene_variant | MODIFIER | c.*3149C>T| |
S40 S49 |
| 147906 | BAA10g32320 | A10 | 23277701 | A | G | downstream_gene_variant | MODIFIER | c.*366A>G| |
S260 |
| 147907 | BAA10g32320 | A10 | 23277929 | G | A | downstream_gene_variant | MODIFIER | c.*594G>A| |
S249 |
| 147908 | BAA10g32330 | A10 | 23279688 | G | A | upstream_gene_variant | MODIFIER | c.-1267C>T| |
S270 |
| 147909 | BAA10g32340 | A10 | 23279885 | C | T | missense_variant | MODERATE | c.1520G>A|p.Gly507Asp |
S196 |
| 147910 | BAA10g32340 | A10 | 23280269 | G | A | missense_variant | MODERATE | c.1372C>T|p.Leu458Phe |
S180 |
| 147911 | BAA10g32340 | A10 | 23280464 | G | A | synonymous_variant | LOW | c.1288C>T|p.Leu430Leu |
S50 |
| 147912 | BAA10g32330 | A10 | 23280875 | G | A | upstream_gene_variant | MODIFIER | c.-2454C>T| |
S241 |
| 147913 | BAA10g32340 | A10 | 23281123 | G | A | missense_variant | MODERATE | c.848C>T|p.Thr283Ile |
S68 |
| 147914 | BAA10g32340 | A10 | 23281264 | G | A | missense_variant | MODERATE | c.707C>T|p.Thr236Ile |
S221 S294 |
| 147915 | BAA10g32330 | A10 | 23282000 | G | A | upstream_gene_variant | MODIFIER | c.-3579C>T| |
S288 |
| 147916 | BAA10g32330 | A10 | 23282153 | G | A | upstream_gene_variant | MODIFIER | c.-3732C>T| |
S57 |
| 147917 | BAA10g32340 | A10 | 23282231 | G | A | missense_variant | MODERATE | c.260C>T|p.Ser87Phe |
S265 |
| 147918 | BAA10g32330 | A10 | 23283336 | G | A | upstream_gene_variant | MODIFIER | c.-4915C>T| |
S179 |
| 147919 | BAA10g32340 | A10 | 23284367 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S153 S213 |
| 147920 | BAA10g32350 | A10 | 23284538 | G | A | synonymous_variant | LOW | c.453G>A|p.Glu151Glu |
S252 |
| 147921 | BAA10g32350 | A10 | 23284593 | G | A | missense_variant | MODERATE | c.508G>A|p.Gly170Arg |
S189 |
| 147922 | BAA10g32350 | A10 | 23284621 | G | A | missense_variant | MODERATE | c.536G>A|p.Arg179Lys |
S199 |
| 147923 | BAA10g32350 | A10 | 23284992 | C | T | synonymous_variant | LOW | c.753C>T|p.His251His |
S146 |
| 147924 | BAA10g32360 | A10 | 23285823 | G | A | missense_variant | MODERATE | c.205G>A|p.Ala69Thr |
S77 S82 |
| 147925 | BAA10g32360 | A10 | 23286333 | G | A | missense_variant | MODERATE | c.715G>A|p.Glu239Lys |
S205 |