| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31801 | BAA01g21990 | A01 | 10962924 | G | C | synonymous_variant | LOW | c.393G>C|p.Ala131Ala |
S91 |
| 31802 | BAA01g21990 | A01 | 10962957 | G | A | synonymous_variant | LOW | c.426G>A|p.Ala142Ala |
S91 |
| 31803 | BAA01g21990 | A01 | 10962970 | A | C | synonymous_variant | LOW | c.439A>C|p.Arg147Arg |
S91 |
| 31804 | BAA01g21990 | A01 | 10962972 | G | T | missense_variant | MODERATE | c.441G>T|p.Arg147Ser |
S91 |
| 31805 | BAA01g21990 | A01 | 10962984 | A | T | synonymous_variant | LOW | c.453A>T|p.Ser151Ser |
S91 |
| 31806 | BAA01g21990 | A01 | 10962990 | G | C | synonymous_variant | LOW | c.459G>C|p.Ala153Ala |
S91 |
| 31807 | BAA01g21990 | A01 | 10962991 | G | A | missense_variant | MODERATE | c.460G>A|p.Val154Ile |
S91 |
| 31808 | BAA01g21990 | A01 | 10963017 | G | T | synonymous_variant | LOW | c.486G>T|p.Ser162Ser |
S91 |
| 31809 | BAA01g21990 | A01 | 10963030 | G | T | missense_variant | MODERATE | c.499G>T|p.Ala167Ser |
S147 S91 |
| 31810 | BAA01g21990 | A01 | 10963032 | T | C | synonymous_variant | LOW | c.501T>C|p.Ala167Ala |
S147 S91 |
| 31811 | BAA01g21990 | A01 | 10963793 | G | A | missense_variant | MODERATE | c.640G>A|p.Ala214Thr |
S32 |
| 31812 | BAA01g21990 | A01 | 10964681 | C | T | downstream_gene_variant | MODIFIER | c.*454C>T| |
S192 |
| 31813 | BAA01g21990 | A01 | 10965536 | G | A | downstream_gene_variant | MODIFIER | c.*1309G>A| |
S71 |
| 31814 | BAA01g21990 | A01 | 10966726 | G | A | downstream_gene_variant | MODIFIER | c.*2499G>A| |
S123 |
| 31815 | BAA01g21990 | A01 | 10967359 | G | A | downstream_gene_variant | MODIFIER | c.*3132G>A| |
S186 |
| 31816 | BAA01g22010 | A01 | 10971223 | G | A | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S100 |
| 31817 | BAA01g22000 | A01 | 10972814 | G | A | stop_gained | HIGH | c.1591C>T|p.Gln531* |
S207 |
| 31818 | BAA01g22000 | A01 | 10973216 | C | T | missense_variant | MODERATE | c.1277G>A|p.Arg426Lys |
S279 |
| 31819 | BAA01g22010 | A01 | 10974296 | G | A | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S122 |
| 31820 | BAA01g22000 | A01 | 10975099 | G | A | missense_variant | MODERATE | c.29C>T|p.Pro10Leu |
S236 |
| 31821 | BAA01g22000 | A01 | 10977890 | G | A | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S194 |
| 31822 | BAA01g22020 | A01 | 10980917 | C | T | upstream_gene_variant | MODIFIER | c.-1194G>A| |
S289 S290 |
| 31823 | BAA01g22020 | A01 | 10982218 | C | T | upstream_gene_variant | MODIFIER | c.-2495G>A| |
S44 |
| 31824 | BAA01g22020 | A01 | 10982606 | G | A | upstream_gene_variant | MODIFIER | c.-2883C>T| |
S27 |
| 31825 | BAA01g22020 | A01 | 10983988 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S109 |