| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 60251 | BAA01g32130 | A01 | 21096382 | C | T | missense_variant | MODERATE | c.1020G>A|p.Met340Ile |
S23 |
| 60252 | BAA01g32130 | A01 | 21096696 | G | A | stop_gained | HIGH | c.706C>T|p.Gln236* |
S95 |
| 60253 | BAA01g32130 | A01 | 21096754 | G | A | synonymous_variant | LOW | c.648C>T|p.Asn216Asn |
S172 S217 |
| 60254 | BAA01g32130 | A01 | 21096872 | G | A | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S284 |
| 60255 | BAA01g32130 | A01 | 21097091 | G | A | missense_variant | MODERATE | c.311C>T|p.Pro104Leu |
S86 |
| 60256 | BAA01g32130 | A01 | 21097256 | G | A | missense_variant | MODERATE | c.146C>T|p.Ser49Phe |
S151 |
| 60257 | BAA01g32130 | A01 | 21099489 | C | T | upstream_gene_variant | MODIFIER | c.-2088G>A| |
S19 |
| 60258 | BAA01g32130 | A01 | 21099591 | C | T | upstream_gene_variant | MODIFIER | c.-2190G>A| |
S120 |
| 60259 | BAA01g32130 | A01 | 21099650 | G | A | upstream_gene_variant | MODIFIER | c.-2249C>T| |
S301 S304 |
| 60260 | BAA01g32130 | A01 | 21100565 | G | A | upstream_gene_variant | MODIFIER | c.-3164C>T| |
S126 |
| 60261 | BAA01g32130 | A01 | 21100663 | C | T | upstream_gene_variant | MODIFIER | c.-3262G>A| |
S87 |
| 60262 | BAA01g32130 | A01 | 21100979 | C | T | upstream_gene_variant | MODIFIER | c.-3578G>A| |
S23 |
| 60263 | BAA01g32140 | A01 | 21101203 | G | A | synonymous_variant | LOW | c.4008C>T|p.Ser1336Ser |
S86 |
| 60264 | BAA01g32140 | A01 | 21101290 | G | A | synonymous_variant | LOW | c.3921C>T|p.Leu1307Leu |
S217 |
| 60265 | BAA01g32140 | A01 | 21101668 | G | A | synonymous_variant | LOW | c.3543C>T|p.Asp1181Asp |
S84 S93 |
| 60266 | BAA01g32140 | A01 | 21102681 | G | A | missense_variant | MODERATE | c.2530C>T|p.Leu844Phe |
S259 |
| 60267 | BAA01g32140 | A01 | 21102923 | C | T | missense_variant | MODERATE | c.2288G>A|p.Arg763Gln |
S51 |
| 60268 | BAA01g32140 | A01 | 21102934 | G | A | synonymous_variant | LOW | c.2277C>T|p.Pro759Pro |
S192 |
| 60269 | BAA01g32140 | A01 | 21103437 | C | T | missense_variant | MODERATE | c.1774G>A|p.Asp592Asn |
S205 |
| 60270 | BAA01g32140 | A01 | 21103561 | C | T | intron_variant | MODIFIER | c.1768+84G>A| |
S249 |
| 60271 | BAA01g32140 | A01 | 21103798 | C | T | missense_variant | MODERATE | c.1615G>A|p.Glu539Lys |
S158 |
| 60272 | BAA01g32140 | A01 | 21103818 | G | A | missense_variant | MODERATE | c.1595C>T|p.Ala532Val |
S252 |
| 60273 | BAA01g32140 | A01 | 21104836 | G | A | stop_gained | HIGH | c.577C>T|p.Gln193* |
S172 S217 |
| 60274 | BAA01g32150 | A01 | 21105264 | G | A | upstream_gene_variant | MODIFIER | c.-4871G>A| |
S283 |
| 60275 | BAA01g32140 | A01 | 21105566 | G | A | upstream_gene_variant | MODIFIER | c.-119C>T| |
S25 |