| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 76551 | BAA01g40430 | A01 | 26803364 | G | A | downstream_gene_variant | MODIFIER | c.*4742G>A| |
S86 |
| 76552 | BAA01g40430 | A01 | 26803393 | C | T | downstream_gene_variant | MODIFIER | c.*4771C>T| |
S16 |
| 76553 | BAA01g40450 | A01 | 26804287 | C | T | missense_variant | MODERATE | c.3707G>A|p.Ser1236Asn |
S7 |
| 76554 | BAA01g40450 | A01 | 26805053 | G | A | missense_variant | MODERATE | c.2941C>T|p.Leu981Phe |
S135 |
| 76555 | BAA01g40450 | A01 | 26805210 | C | T | synonymous_variant | LOW | c.2784G>A|p.Gln928Gln |
S302 |
| 76556 | BAA01g40450 | A01 | 26805751 | C | T | missense_variant | MODERATE | c.2243G>A|p.Arg748Lys |
S153 |
| 76557 | BAA01g40450 | A01 | 26805872 | G | T | missense_variant | MODERATE | c.2122C>A|p.Gln708Lys |
S82 S92 |
| 76558 | BAA01g40460 | A01 | 26806440 | C | T | upstream_gene_variant | MODIFIER | c.-3436C>T| |
S130 |
| 76559 | BAA01g40450 | A01 | 26807005 | G | A | stop_gained | HIGH | c.1393C>T|p.Gln465* |
S177 |
| 76560 | BAA01g40450 | A01 | 26807579 | C | T | stop_gained | HIGH | c.819G>A|p.Trp273* |
S75 S81 |
| 76561 | BAA01g40450 | A01 | 26807924 | C | T | synonymous_variant | LOW | c.474G>A|p.Gln158Gln |
S104 S52 |
| 76562 | BAA01g40450 | A01 | 26808097 | G | A | stop_gained | HIGH | c.301C>T|p.Gln101* |
S255 |
| 76563 | BAA01g40450 | A01 | 26808273 | G | A | missense_variant | MODERATE | c.125C>T|p.Pro42Leu |
S262 |
| 76564 | BAA01g40450 | A01 | 26809588 | G | A | upstream_gene_variant | MODIFIER | c.-1191C>T| |
S202 |
| 76565 | BAA01g40460 | A01 | 26809901 | C | T | missense_variant | MODERATE | c.26C>T|p.Thr9Ile |
S4 |
| 76566 | BAA01g40460 | A01 | 26810760 | G | A | synonymous_variant | LOW | c.885G>A|p.Lys295Lys |
S76 |
| 76567 | BAA01g40460 | A01 | 26810945 | G | A | splice_region_variant&intron_variant | LOW | c.893-6G>A| |
S15 S3 |
| 76568 | BAA01g40460 | A01 | 26811130 | C | T | stop_gained | HIGH | c.1072C>T|p.Arg358* |
S228 |
| 76569 | BAA01g40450 | A01 | 26811538 | C | T | upstream_gene_variant | MODIFIER | c.-3141G>A| |
S164 |
| 76570 | BAA01g40450 | A01 | 26811695 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S87 |
| 76571 | BAA01g40470 | A01 | 26812249 | C | T | missense_variant | MODERATE | c.4748G>A|p.Arg1583Lys |
S184 |
| 76572 | BAA01g40470 | A01 | 26812272 | C | T | stop_gained | HIGH | c.4725G>A|p.Trp1575* |
S85 |
| 76573 | BAA01g40470 | A01 | 26812383 | G | A | synonymous_variant | LOW | c.4614C>T|p.Cys1538Cys |
S35 |
| 76574 | BAA01g40470 | A01 | 26812499 | C | T | splice_donor_variant&intron_variant | HIGH | c.4581+1G>A| |
S84 |
| 76575 | BAA01g40470 | A01 | 26814182 | C | T | splice_donor_variant&intron_variant | HIGH | c.3525+1G>A| |
S28 |