Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g33940 | A07 | 32624567 | C | T | missense_variant | MODERATE | c.2647G>A|p.Ala883Thr |
S292 |
2 | BAA07g33940 | A07 | 32625473 | C | T | synonymous_variant | LOW | c.2091G>A|p.Glu697Glu |
S265 |
3 | BAA07g33940 | A07 | 32625790 | C | T | missense_variant | MODERATE | c.1844G>A|p.Gly615Glu |
S23 |
4 | BAA07g33940 | A07 | 32625994 | G | A | missense_variant | MODERATE | c.1640C>T|p.Ala547Val |
S111 |
5 | BAA07g33940 | A07 | 32626122 | C | T | synonymous_variant | LOW | c.1512G>A|p.Arg504Arg |
S100 |
6 | BAA07g33940 | A07 | 32626187 | C | T | missense_variant | MODERATE | c.1447G>A|p.Glu483Lys |
S216 |
7 | BAA07g33940 | A07 | 32626812 | G | A | synonymous_variant | LOW | c.822C>T|p.Phe274Phe |
S216 S265 S39 |
8 | BAA07g33940 | A07 | 32627716 | G | A | intron_variant | MODIFIER | c.408+125C>T| |
S78 S83 |
9 | BAA07g33940 | A07 | 32628736 | G | A | upstream_gene_variant | MODIFIER | c.-488C>T| |
S17 |
10 | BAA07g33940 | A07 | 32628828 | G | A | upstream_gene_variant | MODIFIER | c.-580C>T| |
S297 |
11 | BAA07g33940 | A07 | 32629396 | G | A | upstream_gene_variant | MODIFIER | c.-1148C>T| |
S40 S49 |
12 | BAA07g33940 | A07 | 32629811 | G | A | upstream_gene_variant | MODIFIER | c.-1563C>T| |
S183 S198 |
13 | BAA07g33940 | A07 | 32630000 | G | A | upstream_gene_variant | MODIFIER | c.-1752C>T| |
S242 |
14 | BAA07g33940 | A07 | 32630245 | G | A | upstream_gene_variant | MODIFIER | c.-1997C>T| |
S111 |
15 | BAA07g33940 | A07 | 32631436 | C | T | upstream_gene_variant | MODIFIER | c.-3188G>A| |
S100 |