| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 20951 | BAA01g15360 | A01 | 7381324 | C | T | upstream_gene_variant | MODIFIER | c.-3077G>A| |
S221 |
| 20952 | BAA01g15360 | A01 | 7383131 | G | A | upstream_gene_variant | MODIFIER | c.-4884C>T| |
S171 |
| 20953 | BAA01g15360-BAA01g15370 | A01 | 7384036 | C | T | intergenic_region | MODIFIER | n.7384036C>T| |
S295 |
| 20954 | BAA01g15360-BAA01g15370 | A01 | 7384673 | G | A | intergenic_region | MODIFIER | n.7384673G>A| |
S280 |
| 20955 | BAA01g15370 | A01 | 7385338 | G | A | downstream_gene_variant | MODIFIER | c.*4632C>T| |
S216 |
| 20956 | BAA01g15370 | A01 | 7385624 | G | A | downstream_gene_variant | MODIFIER | c.*4346C>T| |
S96 |
| 20957 | BAA01g15370 | A01 | 7386914 | C | T | downstream_gene_variant | MODIFIER | c.*3056G>A| |
S223 |
| 20958 | BAA01g15370 | A01 | 7387673 | G | A | downstream_gene_variant | MODIFIER | c.*2297C>T| |
S229 |
| 20959 | BAA01g15370 | A01 | 7387962 | G | A | downstream_gene_variant | MODIFIER | c.*2008C>T| |
S275 |
| 20960 | BAA01g15370 | A01 | 7387969 | C | T | downstream_gene_variant | MODIFIER | c.*2001G>A| |
S16 |
| 20961 | BAA01g15370 | A01 | 7388078 | C | A | downstream_gene_variant | MODIFIER | c.*1892G>T| |
S284 |
| 20962 | BAA01g15370 | A01 | 7388821 | G | A | downstream_gene_variant | MODIFIER | c.*1149C>T| |
S95 |
| 20963 | BAA01g15370 | A01 | 7388824 | C | T | downstream_gene_variant | MODIFIER | c.*1146G>A| |
S134 |
| 20964 | BAA01g15370 | A01 | 7389242 | C | T | downstream_gene_variant | MODIFIER | c.*728G>A| |
S4 |
| 20965 | BAA01g15370 | A01 | 7389616 | C | T | downstream_gene_variant | MODIFIER | c.*354G>A| |
S260 |
| 20966 | BAA01g15370 | A01 | 7389754 | C | T | downstream_gene_variant | MODIFIER | c.*216G>A| |
S265 |
| 20967 | BAA01g15370 | A01 | 7390707 | G | A | missense_variant | MODERATE | c.521C>T|p.Ser174Phe |
S294 |
| 20968 | BAA01g15370 | A01 | 7391028 | G | A | intron_variant | MODIFIER | c.442+141C>T| |
S229 |
| 20969 | BAA01g15370 | A01 | 7393056 | C | T | upstream_gene_variant | MODIFIER | c.-1446G>A| |
S266 |
| 20970 | BAA01g15370 | A01 | 7394898 | T | A | upstream_gene_variant | MODIFIER | c.-3288A>T| |
S205 |
| 20971 | BAA01g15380 | A01 | 7398189 | C | T | synonymous_variant | LOW | c.153C>T|p.Ile51Ile |
S305 |
| 20972 | BAA01g15380 | A01 | 7398404 | T | G | missense_variant | MODERATE | c.368T>G|p.Val123Gly |
S1 |
| 20973 | BAA01g15380 | A01 | 7399089 | G | A | synonymous_variant | LOW | c.1053G>A|p.Arg351Arg |
S293 |
| 20974 | BAA01g15390 | A01 | 7399418 | G | A | synonymous_variant | LOW | c.3096C>T|p.His1032His |
S202 |
| 20975 | BAA01g15380 | A01 | 7401487 | G | A | downstream_gene_variant | MODIFIER | c.*2281G>A| |
S83 S88 |