| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 217901 | BAA02g32750 | A02 | 27986670 | G | A | missense_variant | MODERATE | c.1828G>A|p.Asp610Asn |
S113 |
| 217902 | BAA02g32750 | A02 | 27986834 | G | A | synonymous_variant | LOW | c.1992G>A|p.Ala664Ala |
S134 |
| 217903 | BAA02g32750 | A02 | 27987131 | G | A | synonymous_variant | LOW | c.2289G>A|p.Ser763Ser |
S276 |
| 217904 | BAA02g32750 | A02 | 27987198 | G | A | missense_variant | MODERATE | c.2356G>A|p.Asp786Asn |
S13 |
| 217905 | BAA02g32750 | A02 | 27987299 | G | A | stop_gained | HIGH | c.2457G>A|p.Trp819* |
S247 |
| 217906 | BAA02g32750 | A02 | 27987340 | G | A | missense_variant | MODERATE | c.2498G>A|p.Arg833Lys |
S89 |
| 217907 | BAA02g32750 | A02 | 27987474 | G | A | missense_variant | MODERATE | c.2560G>A|p.Asp854Asn |
S298 |
| 217908 | BAA02g32750 | A02 | 27987499 | C | T | missense_variant | MODERATE | c.2585C>T|p.Ser862Phe |
S118 |
| 217909 | BAA02g32750 | A02 | 27987768 | C | A | intron_variant | MODIFIER | c.2760+94C>A| |
S150 |
| 217910 | BAA02g32750 | A02 | 27987769 | C | T | intron_variant | MODIFIER | c.2760+95C>T| |
S150 |
| 217911 | BAA02g32750 | A02 | 27987890 | C | T | intron_variant | MODIFIER | c.2760+216C>T| |
S18 |
| 217912 | BAA02g32750 | A02 | 27988297 | C | G | intron_variant | MODIFIER | c.2760+623C>G| |
S216 |
| 217913 | BAA02g32750 | A02 | 27988459 | G | A | intron_variant | MODIFIER | c.2761-518G>A| |
S298 |
| 217914 | BAA02g32750 | A02 | 27988787 | G | A | intron_variant | MODIFIER | c.2761-190G>A| |
S149 |
| 217915 | BAA02g32750 | A02 | 27988832 | G | A | intron_variant | MODIFIER | c.2761-145G>A| |
S11 |
| 217916 | BAA02g32750 | A02 | 27989217 | T | G | missense_variant | MODERATE | c.3001T>G|p.Leu1001Val |
S39 |
| 217917 | BAA02g32750 | A02 | 27989383 | G | A | intron_variant | MODIFIER | c.3115+52G>A| |
S86 |
| 217918 | BAA02g32750 | A02 | 27989539 | G | A | intron_variant | MODIFIER | c.3115+208G>A| |
S223 |
| 217919 | BAA02g32750 | A02 | 27989859 | C | T | intron_variant | MODIFIER | c.3116-286C>T| |
S157 S163 |
| 217920 | BAA02g32750 | A02 | 27990133 | C | T | intron_variant | MODIFIER | c.3116-12C>T| |
S233 |
| 217921 | BAA02g32750 | A02 | 27990241 | G | A | missense_variant | MODERATE | c.3212G>A|p.Arg1071Lys |
S146 |
| 217922 | BAA02g32750 | A02 | 27990304 | C | T | missense_variant | MODERATE | c.3275C>T|p.Ser1092Phe |
S175 |
| 217923 | BAA02g32750 | A02 | 27990340 | G | A | missense_variant | MODERATE | c.3311G>A|p.Gly1104Glu |
S188 |
| 217924 | BAA02g32750 | A02 | 27991784 | G | A | missense_variant | MODERATE | c.3928G>A|p.Asp1310Asn |
S80 |
| 217925 | BAA02g32750 | A02 | 27994769 | G | A | intron_variant | MODIFIER | c.4253+2401G>A| |
S247 |