Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g17450 | A07 | 23804572 | G | A | synonymous_variant | LOW | c.2766C>T|p.Phe922Phe |
S239 |
2 | BAA07g17450 | A07 | 23804588 | G | A | missense_variant | MODERATE | c.2750C>T|p.Ala917Val |
S50 S95 |
3 | BAA07g17450 | A07 | 23804860 | G | A | splice_region_variant&intron_variant | LOW | c.2565-3C>T| |
S100 |
4 | BAA07g17450 | A07 | 23806519 | G | A | missense_variant | MODERATE | c.1664C>T|p.Pro555Leu |
S158 |
5 | BAA07g17450 | A07 | 23807001 | G | A | missense_variant | MODERATE | c.1423C>T|p.Pro475Ser |
S209 |
6 | BAA07g17450 | A07 | 23807557 | G | A | missense_variant | MODERATE | c.1043C>T|p.Pro348Leu |
S71 |
7 | BAA07g17450 | A07 | 23807749 | C | T | synonymous_variant | LOW | c.942G>A|p.Thr314Thr |
S36 |
8 | BAA07g17450 | A07 | 23809066 | C | T | missense_variant | MODERATE | c.25G>A|p.Ala9Thr |
S68 |
9 | BAA07g17450 | A07 | 23810143 | G | A | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S238 |
10 | BAA07g17450 | A07 | 23810207 | G | A | upstream_gene_variant | MODIFIER | c.-1117C>T| |
S80 |
11 | BAA07g17450 | A07 | 23810243 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S306 S308 |
12 | BAA07g17450 | A07 | 23812198 | C | T | upstream_gene_variant | MODIFIER | c.-3108G>A| |
S275 |
13 | BAA07g17450 | A07 | 23812991 | G | A | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S140 |