Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g57210 | A09 | 56572504 | C | T | downstream_gene_variant | MODIFIER | c.*1366G>A| |
S51 |
2 | BAA09g57210 | A09 | 56574270 | G | A | missense_variant | MODERATE | c.2846C>T|p.Thr949Ile |
S140 S64 S72 |
3 | BAA09g57210 | A09 | 56574297 | C | T | missense_variant | MODERATE | c.2819G>A|p.Arg940Lys |
S153 S157 S166 S167 S236 S257 S262 |
4 | BAA09g57210 | A09 | 56575685 | C | T | synonymous_variant | LOW | c.2031G>A|p.Lys677Lys |
S87 |
5 | BAA09g57210 | A09 | 56576467 | G | A | synonymous_variant | LOW | c.1441C>T|p.Leu481Leu |
S48 |
6 | BAA09g57210 | A09 | 56576744 | G | A | missense_variant | MODERATE | c.1249C>T|p.Arg417Cys |
S59 |
7 | BAA09g57210 | A09 | 56578713 | G | A | missense_variant | MODERATE | c.46C>T|p.Pro16Ser |
S288 |
8 | BAA09g57210 | A09 | 56579779 | G | A | upstream_gene_variant | MODIFIER | c.-1021C>T| |
S135 |
9 | BAA09g57210 | A09 | 56580047 | C | T | upstream_gene_variant | MODIFIER | c.-1289G>A| |
S303 |
10 | BAA09g57210 | A09 | 56581290 | G | A | upstream_gene_variant | MODIFIER | c.-2532C>T| |
S271 |
11 | BAA09g57210 | A09 | 56582829 | C | T | upstream_gene_variant | MODIFIER | c.-4071G>A| |
S8 |
12 | BAA09g57210 | A09 | 56583152 | G | A | upstream_gene_variant | MODIFIER | c.-4394C>T| |
S107 |
13 | BAA09g57210 | A09 | 56583488 | C | T | upstream_gene_variant | MODIFIER | c.-4730G>A| |
S239 |