Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01660 | A07 | 1181586 | G | A | downstream_gene_variant | MODIFIER | c.*979C>T| |
S139 |
2 | BAA07g01660 | A07 | 1182613 | G | A | synonymous_variant | LOW | c.1794C>T|p.Ala598Ala |
S241 |
3 | BAA07g01660 | A07 | 1183295 | C | T | missense_variant | MODERATE | c.1600G>A|p.Asp534Asn |
S297 |
4 | BAA07g01660 | A07 | 1183741 | G | A | synonymous_variant | LOW | c.1329C>T|p.Pro443Pro |
S266 |
5 | BAA07g01660 | A07 | 1184226 | G | A | missense_variant | MODERATE | c.844C>T|p.Arg282Trp |
S63 |
6 | BAA07g01660 | A07 | 1185079 | G | A | upstream_gene_variant | MODIFIER | c.-10C>T| |
S142 |
7 | BAA07g01660 | A07 | 1185492 | C | T | upstream_gene_variant | MODIFIER | c.-423G>A| |
S27 |
8 | BAA07g01660 | A07 | 1186514 | G | A | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S262 |
9 | BAA07g01660 | A07 | 1186679 | C | T | upstream_gene_variant | MODIFIER | c.-1610G>A| |
S174 S216 |
10 | BAA07g01660 | A07 | 1188609 | G | A | upstream_gene_variant | MODIFIER | c.-3540C>T| |
S263 |
11 | BAA07g01660 | A07 | 1189310 | C | T | upstream_gene_variant | MODIFIER | c.-4241G>A| |
S189 |