| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 73501 | BAA01g38520 | A01 | 25703288 | G | A | missense_variant | MODERATE | c.377C>T|p.Ser126Phe |
S209 |
| 73502 | BAA01g38520 | A01 | 25703654 | G | A | missense_variant | MODERATE | c.11C>T|p.Pro4Leu |
S229 |
| 73503 | BAA01g38520 | A01 | 25703655 | G | A | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S135 |
| 73504 | BAA01g38510 | A01 | 25704429 | C | T | upstream_gene_variant | MODIFIER | c.-3475G>A| |
S82 S92 |
| 73505 | BAA01g38510 | A01 | 25704702 | C | T | upstream_gene_variant | MODIFIER | c.-3748G>A| |
S4 |
| 73506 | BAA01g38520 | A01 | 25706133 | C | T | upstream_gene_variant | MODIFIER | c.-2469G>A| |
S244 |
| 73507 | BAA01g38520 | A01 | 25706270 | G | A | upstream_gene_variant | MODIFIER | c.-2606C>T| |
S265 |
| 73508 | BAA01g38520 | A01 | 25707982 | C | T | upstream_gene_variant | MODIFIER | c.-4318G>A| |
S198 |
| 73509 | BAA01g38530 | A01 | 25709188 | C | T | missense_variant | MODERATE | c.626C>T|p.Thr209Met |
S7 |
| 73510 | BAA01g38540 | A01 | 25709493 | C | T | upstream_gene_variant | MODIFIER | c.-708C>T| |
S69 |
| 73511 | BAA01g38540 | A01 | 25709678 | C | T | upstream_gene_variant | MODIFIER | c.-523C>T| |
S16 S181 S56 |
| 73512 | BAA01g38540 | A01 | 25710228 | C | T | missense_variant | MODERATE | c.28C>T|p.Leu10Phe |
S233 |
| 73513 | BAA01g38550 | A01 | 25712280 | C | T | missense_variant | MODERATE | c.304G>A|p.Asp102Asn |
S82 S92 |
| 73514 | BAA01g38550 | A01 | 25713337 | G | A | upstream_gene_variant | MODIFIER | c.-262C>T| |
S292 |
| 73515 | BAA01g38550 | A01 | 25713758 | G | A | upstream_gene_variant | MODIFIER | c.-683C>T| |
S225 |
| 73516 | BAA01g38550 | A01 | 25715314 | G | A | upstream_gene_variant | MODIFIER | c.-2239C>T| |
S281 |
| 73517 | BAA01g38550 | A01 | 25715449 | C | T | upstream_gene_variant | MODIFIER | c.-2374G>A| |
S42 |
| 73518 | BAA01g38550 | A01 | 25715948 | G | A | upstream_gene_variant | MODIFIER | c.-2873C>T| |
S116 |
| 73519 | BAA01g38550 | A01 | 25716022 | C | T | upstream_gene_variant | MODIFIER | c.-2947G>A| |
S293 |
| 73520 | BAA01g38550 | A01 | 25716417 | G | A | upstream_gene_variant | MODIFIER | c.-3342C>T| |
S107 |
| 73521 | BAA01g38550 | A01 | 25717795 | C | T | upstream_gene_variant | MODIFIER | c.-4720G>A| |
S210 |
| 73522 | BAA01g38570 | A01 | 25718463 | G | A | upstream_gene_variant | MODIFIER | c.-4382G>A| |
S6 |
| 73523 | BAA01g38570 | A01 | 25718780 | C | T | upstream_gene_variant | MODIFIER | c.-4065C>T| |
S100 |
| 73524 | BAA01g38560 | A01 | 25718885 | G | A | missense_variant | MODERATE | c.443C>T|p.Pro148Leu |
S221 |
| 73525 | BAA01g38560 | A01 | 25719090 | G | A | missense_variant | MODERATE | c.325C>T|p.Pro109Ser |
S60 |