| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157951 | BAA02g05600 | A02 | 2417474 | G | A | missense_variant | MODERATE | c.1261C>T|p.Arg421Cys |
S67 |
| 157952 | BAA02g05600 | A02 | 2417476 | G | A | missense_variant | MODERATE | c.1259C>T|p.Ala420Val |
S286 |
| 157953 | BAA02g05600 | A02 | 2417658 | G | A | synonymous_variant | LOW | c.1077C>T|p.Val359Val |
S190 |
| 157954 | BAA02g05600 | A02 | 2417676 | C | T | synonymous_variant | LOW | c.1059G>A|p.Gly353Gly |
S202 |
| 157955 | BAA02g05600 | A02 | 2418213 | G | A | synonymous_variant | LOW | c.522C>T|p.His174His |
S176 |
| 157956 | BAA02g05600 | A02 | 2418707 | C | T | missense_variant | MODERATE | c.28G>A|p.Asp10Asn |
S243 S299 |
| 157957 | BAA02g05590 | A02 | 2418787 | G | A | upstream_gene_variant | MODIFIER | c.-3999C>T| |
S186 |
| 157958 | BAA02g05590 | A02 | 2419167 | C | T | upstream_gene_variant | MODIFIER | c.-4379G>A| |
S167 |
| 157959 | BAA02g05590 | A02 | 2419179 | G | A | upstream_gene_variant | MODIFIER | c.-4391C>T| |
S131 |
| 157960 | BAA02g05590 | A02 | 2419287 | C | T | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S250 |
| 157961 | BAA02g05600 | A02 | 2420050 | G | A | upstream_gene_variant | MODIFIER | c.-1316C>T| |
S241 |
| 157962 | BAA02g05610 | A02 | 2420858 | C | T | synonymous_variant | LOW | c.210C>T|p.Arg70Arg |
S138 |
| 157963 | BAA02g05600 | A02 | 2421744 | C | T | upstream_gene_variant | MODIFIER | c.-3010G>A| |
S292 |
| 157964 | BAA02g05600 | A02 | 2422392 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S130 |
| 157965 | BAA02g05620 | A02 | 2422580 | G | A | synonymous_variant | LOW | c.270G>A|p.Glu90Glu |
S4 |
| 157966 | BAA02g05600 | A02 | 2423367 | G | A | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S223 |
| 157967 | BAA02g05600 | A02 | 2423732 | G | A | upstream_gene_variant | MODIFIER | c.-4998C>T| |
S199 |
| 157968 | BAA02g05640 | A02 | 2423838 | G | A | upstream_gene_variant | MODIFIER | c.-4159G>A| |
S182 S292 |
| 157969 | BAA02g05630 | A02 | 2424469 | G | A | missense_variant | MODERATE | c.884C>T|p.Pro295Leu |
S164 |
| 157970 | BAA02g05630 | A02 | 2426459 | C | T | upstream_gene_variant | MODIFIER | c.-443G>A| |
S37 |
| 157971 | BAA02g05630 | A02 | 2426698 | C | T | upstream_gene_variant | MODIFIER | c.-682G>A| |
S201 |
| 157972 | BAA02g05630 | A02 | 2427159 | G | A | upstream_gene_variant | MODIFIER | c.-1143C>T| |
S279 |
| 157973 | BAA02g05640 | A02 | 2429030 | G | A | missense_variant | MODERATE | c.1034G>A|p.Gly345Glu |
S133 |
| 157974 | BAA02g05640 | A02 | 2429173 | G | A | missense_variant | MODERATE | c.1177G>A|p.Val393Ile |
S265 |
| 157975 | BAA02g05650 | A02 | 2431482 | C | T | upstream_gene_variant | MODIFIER | c.-381C>T| |
S180 |