| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 74951 | BAA01g39480 | A01 | 26244111 | A | T | upstream_gene_variant | MODIFIER | c.-4957A>T| |
S220 |
| 74952 | BAA01g39480 | A01 | 26245168 | C | T | upstream_gene_variant | MODIFIER | c.-3900C>T| |
S32 |
| 74953 | BAA01g39480 | A01 | 26245245 | C | T | upstream_gene_variant | MODIFIER | c.-3823C>T| |
S174 S27 |
| 74954 | BAA01g39480 | A01 | 26245284 | C | A | upstream_gene_variant | MODIFIER | c.-3784C>A| |
S221 |
| 74955 | BAA01g39480 | A01 | 26245481 | G | A | upstream_gene_variant | MODIFIER | c.-3587G>A| |
S87 |
| 74956 | BAA01g39480 | A01 | 26246807 | C | T | upstream_gene_variant | MODIFIER | c.-2261C>T| |
S210 |
| 74957 | BAA01g39480 | A01 | 26252255 | C | T | synonymous_variant | LOW | c.1356C>T|p.Ser452Ser |
S256 |
| 74958 | BAA01g39480 | A01 | 26253077 | G | A | downstream_gene_variant | MODIFIER | c.*399G>A| |
S262 |
| 74959 | BAA01g39480 | A01 | 26253641 | G | A | downstream_gene_variant | MODIFIER | c.*963G>A| |
S217 S248 |
| 74960 | BAA01g39480 | A01 | 26253802 | C | T | downstream_gene_variant | MODIFIER | c.*1124C>T| |
S112 |
| 74961 | BAA01g39480 | A01 | 26253867 | C | T | downstream_gene_variant | MODIFIER | c.*1189C>T| |
S209 |
| 74962 | BAA01g39480 | A01 | 26253936 | G | A | downstream_gene_variant | MODIFIER | c.*1258G>A| |
S142 S177 S201 |
| 74963 | BAA01g39480 | A01 | 26254161 | C | T | downstream_gene_variant | MODIFIER | c.*1483C>T| |
S239 |
| 74964 | BAA01g39490 | A01 | 26254444 | G | A | upstream_gene_variant | MODIFIER | c.-4760G>A| |
S47 |
| 74965 | BAA01g39490 | A01 | 26255466 | C | T | upstream_gene_variant | MODIFIER | c.-3738C>T| |
S261 |
| 74966 | BAA01g39490 | A01 | 26255476 | G | A | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S143 |
| 74967 | BAA01g39490 | A01 | 26256226 | G | A | upstream_gene_variant | MODIFIER | c.-2978G>A| |
S143 S150 |
| 74968 | BAA01g39490 | A01 | 26256425 | A | T | upstream_gene_variant | MODIFIER | c.-2779A>T| |
S261 |
| 74969 | BAA01g39490 | A01 | 26257060 | C | A | upstream_gene_variant | MODIFIER | c.-2144C>A| |
S160 |
| 74970 | BAA01g39490 | A01 | 26257751 | G | A | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S284 |
| 74971 | BAA01g39490 | A01 | 26259449 | G | A | synonymous_variant | LOW | c.246G>A|p.Ala82Ala |
S262 |
| 74972 | BAA01g39490 | A01 | 26259825 | G | A | intron_variant | MODIFIER | c.484+138G>A| |
S202 |
| 74973 | BAA01g39490 | A01 | 26260937 | C | T | downstream_gene_variant | MODIFIER | c.*114C>T| |
S54 |
| 74974 | BAA01g39500 | A01 | 26261934 | G | A | upstream_gene_variant | MODIFIER | c.-4572G>A| |
S293 |
| 74975 | BAA01g39500 | A01 | 26263177 | G | A | upstream_gene_variant | MODIFIER | c.-3329G>A| |
S157 S163 |