| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 40001 | BAA01g25440 | A01 | 13817950 | G | A | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S90 |
| 40002 | BAA01g25440 | A01 | 13821077 | G | A | upstream_gene_variant | MODIFIER | c.-3117C>T| |
S100 |
| 40003 | BAA01g25450 | A01 | 13823335 | C | T | missense_variant | MODERATE | c.529C>T|p.Leu177Phe |
S42 |
| 40004 | BAA01g25450 | A01 | 13824017 | C | T | missense_variant | MODERATE | c.1211C>T|p.Ser404Phe |
S133 |
| 40005 | BAA01g25450 | A01 | 13824124 | G | A | missense_variant | MODERATE | c.1318G>A|p.Asp440Asn |
S296 |
| 40006 | BAA01g25450 | A01 | 13825063 | G | A | splice_region_variant&stop_retained_variant | LOW | c.2168G>A|p.Ter723Ter |
S259 |
| 40007 | BAA01g25460 | A01 | 13825481 | G | A | upstream_gene_variant | MODIFIER | c.-4608G>A| |
S240 |
| 40008 | BAA01g25460 | A01 | 13826228 | G | A | upstream_gene_variant | MODIFIER | c.-3861G>A| |
S7 |
| 40009 | BAA01g25460 | A01 | 13826467 | G | A | upstream_gene_variant | MODIFIER | c.-3622G>A| |
S173 |
| 40010 | BAA01g25460 | A01 | 13826993 | G | A | upstream_gene_variant | MODIFIER | c.-3096G>A| |
S208 S219 |
| 40011 | BAA01g25460 | A01 | 13827029 | C | T | upstream_gene_variant | MODIFIER | c.-3060C>T| |
S130 |
| 40012 | BAA01g25460 | A01 | 13827079 | C | T | upstream_gene_variant | MODIFIER | c.-3010C>T| |
S69 |
| 40013 | BAA01g25460 | A01 | 13828004 | T | A | upstream_gene_variant | MODIFIER | c.-2085T>A| |
S153 |
| 40014 | BAA01g25460 | A01 | 13828079 | C | T | upstream_gene_variant | MODIFIER | c.-2010C>T| |
S295 |
| 40015 | BAA01g25460 | A01 | 13828245 | G | A | upstream_gene_variant | MODIFIER | c.-1844G>A| |
S129 |
| 40016 | BAA01g25460 | A01 | 13828494 | G | A | upstream_gene_variant | MODIFIER | c.-1595G>A| |
S56 |
| 40017 | BAA01g25460 | A01 | 13830344 | G | A | missense_variant | MODERATE | c.256G>A|p.Ala86Thr |
S100 |
| 40018 | BAA01g25460 | A01 | 13831101 | G | A | missense_variant | MODERATE | c.1013G>A|p.Arg338Lys |
S32 |
| 40019 | BAA01g25460 | A01 | 13831344 | C | T | missense_variant | MODERATE | c.1256C>T|p.Ala419Val |
S148 S30 S31 |
| 40020 | BAA01g25460 | A01 | 13831370 | G | A | missense_variant | MODERATE | c.1282G>A|p.Glu428Lys |
S288 |
| 40021 | BAA01g25470 | A01 | 13832193 | C | T | upstream_gene_variant | MODIFIER | c.-2422C>T| |
S38 |
| 40022 | BAA01g25470 | A01 | 13832650 | C | T | upstream_gene_variant | MODIFIER | c.-1965C>T| |
S20 |
| 40023 | BAA01g25470 | A01 | 13833223 | G | A | upstream_gene_variant | MODIFIER | c.-1392G>A| |
S180 |
| 40024 | BAA01g25470 | A01 | 13833318 | C | T | upstream_gene_variant | MODIFIER | c.-1297C>T| |
S183 |
| 40025 | BAA01g25470 | A01 | 13834517 | C | T | upstream_gene_variant | MODIFIER | c.-98C>T| |
S210 S225 |