Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30440 | A01 | 19419529 | G | A | upstream_gene_variant | MODIFIER | c.-4263G>A| |
S244 |
2 | BAA01g30440 | A01 | 19420705 | C | T | upstream_gene_variant | MODIFIER | c.-3087C>T| |
S182 |
3 | BAA01g30440 | A01 | 19421557 | G | A | upstream_gene_variant | MODIFIER | c.-2235G>A| |
S229 |
4 | BAA01g30440 | A01 | 19421669 | C | T | upstream_gene_variant | MODIFIER | c.-2123C>T| |
S94 |
5 | BAA01g30440 | A01 | 19422551 | G | A | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S294 |
6 | BAA01g30440 | A01 | 19422811 | C | T | upstream_gene_variant | MODIFIER | c.-981C>T| |
S186 |
7 | BAA01g30440 | A01 | 19423549 | C | T | upstream_gene_variant | MODIFIER | c.-243C>T| |
S42 |
8 | BAA01g30440 | A01 | 19423966 | G | A | missense_variant | MODERATE | c.175G>A|p.Gly59Arg |
S265 |
9 | BAA01g30440 | A01 | 19423967 | G | A | missense_variant | MODERATE | c.176G>A|p.Gly59Glu |
S96 |
10 | BAA01g30440 | A01 | 19424573 | G | A | missense_variant | MODERATE | c.706G>A|p.Ala236Thr |
S221 |
11 | BAA01g30440 | A01 | 19425153 | C | T | missense_variant | MODERATE | c.1286C>T|p.Ala429Val |
S182 |
12 | BAA01g30440 | A01 | 19426511 | C | T | downstream_gene_variant | MODIFIER | c.*1165C>T| |
S88 |
13 | BAA01g30440 | A01 | 19426707 | G | A | downstream_gene_variant | MODIFIER | c.*1361G>A| |
S121 |
14 | BAA01g30440 | A01 | 19426954 | A | T | downstream_gene_variant | MODIFIER | c.*1608A>T| |
S99 |
15 | BAA01g30440 | A01 | 19427363 | C | T | downstream_gene_variant | MODIFIER | c.*2017C>T| |
S142 |
16 | BAA01g30440 | A01 | 19428376 | C | T | downstream_gene_variant | MODIFIER | c.*3030C>T| |
S18 |
17 | BAA01g30440 | A01 | 19428389 | C | T | downstream_gene_variant | MODIFIER | c.*3043C>T| |
S166 |
18 | BAA01g30440 | A01 | 19428423 | G | A | downstream_gene_variant | MODIFIER | c.*3077G>A| |
S163 |