Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g67140 | A03 | 41618746 | C | T | missense_variant | MODERATE | c.1142G>A|p.Ser381Asn |
S100 |
2 | BAA03g67140 | A03 | 41619062 | C | T | splice_region_variant&intron_variant | LOW | c.1059+7G>A| |
S58 |
3 | BAA03g67140 | A03 | 41621887 | G | A | intron_variant | MODIFIER | c.268-715C>T| |
S60 |
4 | BAA03g67140 | A03 | 41622163 | C | T | intron_variant | MODIFIER | c.268-991G>A| |
S174 |
5 | BAA03g67140 | A03 | 41622782 | G | A | intron_variant | MODIFIER | c.268-1610C>T| |
S268 |
6 | BAA03g67140 | A03 | 41623927 | G | A | intron_variant | MODIFIER | c.267+1198C>T| |
S6 |
7 | BAA03g67140 | A03 | 41624768 | G | A | intron_variant | MODIFIER | c.267+357C>T| |
S245 |
8 | BAA03g67140 | A03 | 41624803 | G | A | intron_variant | MODIFIER | c.267+322C>T| |
S132 S137 S215 S89 |
9 | BAA03g67140 | A03 | 41625860 | C | T | upstream_gene_variant | MODIFIER | c.-469G>A| |
S175 |
10 | BAA03g67140 | A03 | 41626145 | A | T | upstream_gene_variant | MODIFIER | c.-754T>A| |
S121 |
11 | BAA03g67140 | A03 | 41627275 | C | T | upstream_gene_variant | MODIFIER | c.-1884G>A| |
S20 |
12 | BAA03g67140 | A03 | 41627277 | C | T | upstream_gene_variant | MODIFIER | c.-1886G>A| |
S256 |
13 | BAA03g67140 | A03 | 41628063 | C | T | upstream_gene_variant | MODIFIER | c.-2672G>A| |
S281 |
14 | BAA03g67140 | A03 | 41628106 | C | T | upstream_gene_variant | MODIFIER | c.-2715G>A| |
S252 |
15 | BAA03g67140 | A03 | 41629660 | G | A | upstream_gene_variant | MODIFIER | c.-4269C>T| |
S25 |