| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 75801 | BAA01g39900 | A01 | 26507749 | C | T | synonymous_variant | LOW | c.153C>T|p.Tyr51Tyr |
S17 |
| 75802 | BAA01g39900 | A01 | 26508323 | C | T | synonymous_variant | LOW | c.402C>T|p.Asp134Asp |
S270 |
| 75803 | BAA01g39900 | A01 | 26508347 | C | T | synonymous_variant | LOW | c.426C>T|p.Thr142Thr |
S160 |
| 75804 | BAA01g39900 | A01 | 26508365 | C | T | synonymous_variant | LOW | c.444C>T|p.Asn148Asn |
S148 S30 S31 |
| 75805 | BAA01g39900 | A01 | 26508621 | G | A | missense_variant | MODERATE | c.700G>A|p.Glu234Lys |
S13 S140 S168 S64 |
| 75806 | BAA01g39900 | A01 | 26508893 | G | A | synonymous_variant | LOW | c.972G>A|p.Ser324Ser |
S245 |
| 75807 | BAA01g39910 | A01 | 26510245 | C | T | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S255 |
| 75808 | BAA01g39910 | A01 | 26513476 | G | A | upstream_gene_variant | MODIFIER | c.-453G>A| |
S260 |
| 75809 | BAA01g39910 | A01 | 26514123 | C | T | synonymous_variant | LOW | c.114C>T|p.Leu38Leu |
S136 |
| 75810 | BAA01g39920 | A01 | 26515141 | C | T | missense_variant | MODERATE | c.1810G>A|p.Gly604Arg |
S120 |
| 75811 | BAA01g39920 | A01 | 26515476 | G | A | missense_variant | MODERATE | c.1475C>T|p.Ser492Phe |
S105 |
| 75812 | BAA01g39920 | A01 | 26515532 | C | T | synonymous_variant | LOW | c.1419G>A|p.Gln473Gln |
S303 |
| 75813 | BAA01g39920 | A01 | 26515772 | G | A | missense_variant | MODERATE | c.1271C>T|p.Ser424Phe |
S45 |
| 75814 | BAA01g39910 | A01 | 26515969 | C | T | downstream_gene_variant | MODIFIER | c.*1747C>T| |
S69 |
| 75815 | BAA01g39920 | A01 | 26516088 | G | A | missense_variant | MODERATE | c.1123C>T|p.His375Tyr |
S160 |
| 75816 | BAA01g39920 | A01 | 26518011 | C | T | missense_variant | MODERATE | c.364G>A|p.Gly122Ser |
S48 |
| 75817 | BAA01g39920 | A01 | 26520016 | C | T | intron_variant | MODIFIER | c.46-1349G>A| |
S134 |
| 75818 | BAA01g39920 | A01 | 26520899 | C | T | intron_variant | MODIFIER | c.46-2232G>A| |
S182 |
| 75819 | BAA01g39920 | A01 | 26523066 | G | A | intron_variant | MODIFIER | c.46-4399C>T| |
S281 |
| 75820 | BAA01g39920 | A01 | 26523125 | C | T | intron_variant | MODIFIER | c.46-4458G>A| |
S293 |
| 75821 | BAA01g39920 | A01 | 26523775 | G | A | intron_variant | MODIFIER | c.45+3942C>T| |
S71 |
| 75822 | BAA01g39920 | A01 | 26524477 | C | T | intron_variant | MODIFIER | c.45+3240G>A| |
S289 S290 |
| 75823 | BAA01g39930 | A01 | 26526498 | C | T | upstream_gene_variant | MODIFIER | c.-3687C>T| |
S165 |
| 75824 | BAA01g39930 | A01 | 26526797 | C | T | upstream_gene_variant | MODIFIER | c.-3388C>T| |
S275 |
| 75825 | BAA01g39930 | A01 | 26527095 | C | T | upstream_gene_variant | MODIFIER | c.-3090C>T| |
S167 |