Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00100 | A05 | 41367 | C | T | upstream_gene_variant | MODIFIER | c.-3851C>T| |
S181 |
2 | BAA05g00100 | A05 | 42040 | G | A | upstream_gene_variant | MODIFIER | c.-3178G>A| |
S298 |
3 | BAA05g00100 | A05 | 42237 | C | T | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S231 |
4 | BAA05g00100 | A05 | 43181 | G | A | upstream_gene_variant | MODIFIER | c.-2037G>A| |
S178 |
5 | BAA05g00100 | A05 | 43402 | G | A | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S223 |
6 | BAA05g00100 | A05 | 43625 | C | T | upstream_gene_variant | MODIFIER | c.-1593C>T| |
S43 |
7 | BAA05g00100 | A05 | 43910 | G | A | upstream_gene_variant | MODIFIER | c.-1308G>A| |
S33 |
8 | BAA05g00100 | A05 | 46882 | G | A | synonymous_variant | LOW | c.858G>A|p.Leu286Leu |
S125 |
9 | BAA05g00100 | A05 | 47586 | C | T | missense_variant&splice_region_variant | MODERATE | c.992C>T|p.Pro331Leu |
S251 |
10 | BAA05g00100 | A05 | 48093 | G | A | synonymous_variant | LOW | c.1290G>A|p.Gly430Gly |
S148 S210 |
11 | BAA05g00100 | A05 | 50612 | G | A | missense_variant | MODERATE | c.2813G>A|p.Cys938Tyr |
S39 |
12 | BAA05g00100 | A05 | 50625 | C | T | synonymous_variant | LOW | c.2826C>T|p.Val942Val |
S171 |
13 | BAA05g00100 | A05 | 51237 | C | T | synonymous_variant | LOW | c.3438C>T|p.Leu1146Leu |
S250 |
14 | BAA05g00100 | A05 | 51441 | C | T | missense_variant | MODERATE | c.3541C>T|p.Arg1181Trp |
S271 |
15 | BAA05g00100 | A05 | 51886 | C | T | missense_variant | MODERATE | c.3986C>T|p.Thr1329Ile |
S110 |
16 | BAA05g00100 | A05 | 52467 | G | A | missense_variant | MODERATE | c.4567G>A|p.Glu1523Lys |
S95 |
17 | BAA05g00100 | A05 | 52817 | G | A | stop_gained | HIGH | c.4917G>A|p.Trp1639* |
S138 |
18 | BAA05g00100 | A05 | 52993 | C | T | missense_variant | MODERATE | c.5093C>T|p.Ala1698Val |
S251 |
19 | BAA05g00100 | A05 | 53019 | C | T | missense_variant | MODERATE | c.5119C>T|p.Pro1707Ser |
S293 |
20 | BAA05g00100 | A05 | 53356 | G | A | missense_variant | MODERATE | c.5456G>A|p.Gly1819Glu |
S281 |
21 | BAA05g00100 | A05 | 53671 | C | T | missense_variant | MODERATE | c.5771C>T|p.Ser1924Phe |
S211 S227 |
22 | BAA05g00100 | A05 | 55282 | C | T | synonymous_variant | LOW | c.6972C>T|p.Phe2324Phe |
S237 |
23 | BAA05g00100 | A05 | 55946 | G | A | stop_gained | HIGH | c.7386G>A|p.Trp2462* |
S166 |
24 | BAA05g00100 | A05 | 58869 | G | A | downstream_gene_variant | MODIFIER | c.*2854G>A| |
S32 |
25 | BAA05g00100 | A05 | 59273 | G | A | downstream_gene_variant | MODIFIER | c.*3258G>A| |
S117 |