Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43960 | A01 | 29088567 | C | T | upstream_gene_variant | MODIFIER | c.-3715C>T| |
S66 |
2 | BAA01g43960 | A01 | 29089610 | G | A | upstream_gene_variant | MODIFIER | c.-2672G>A| |
S117 |
3 | BAA01g43960 | A01 | 29090402 | G | T | upstream_gene_variant | MODIFIER | c.-1880G>T| |
S71 |
4 | BAA01g43960 | A01 | 29090404 | T | G | upstream_gene_variant | MODIFIER | c.-1878T>G| |
S71 |
5 | BAA01g43960 | A01 | 29090440 | G | A | upstream_gene_variant | MODIFIER | c.-1842G>A| |
S291 |
6 | BAA01g43960 | A01 | 29090477 | C | T | upstream_gene_variant | MODIFIER | c.-1805C>T| |
S270 |
7 | BAA01g43960 | A01 | 29092348 | G | A | missense_variant | MODERATE | c.67G>A|p.Ala23Thr |
S182 |
8 | BAA01g43960 | A01 | 29092475 | G | A | missense_variant | MODERATE | c.194G>A|p.Arg65Lys |
S125 |
9 | BAA01g43960 | A01 | 29092611 | G | A | missense_variant | MODERATE | c.253G>A|p.Val85Ile |
S302 |
10 | BAA01g43960 | A01 | 29092825 | C | T | synonymous_variant | LOW | c.378C>T|p.Tyr126Tyr |
S259 |
11 | BAA01g43960 | A01 | 29093214 | G | A | missense_variant&splice_region_variant | MODERATE | c.547G>A|p.Glu183Lys |
S278 |
12 | BAA01g43960 | A01 | 29093302 | C | T | splice_region_variant&intron_variant | LOW | c.550-3C>T| |
S298 |
13 | BAA01g43960 | A01 | 29093870 | G | A | missense_variant | MODERATE | c.895G>A|p.Ala299Thr |
S252 |
14 | BAA01g43960 | A01 | 29093893 | G | A | synonymous_variant | LOW | c.918G>A|p.Lys306Lys |
S98 |
15 | BAA01g43960 | A01 | 29094047 | G | A | missense_variant | MODERATE | c.995G>A|p.Gly332Glu |
S149 |
16 | BAA01g43960 | A01 | 29096190 | C | T | synonymous_variant | LOW | c.1998C>T|p.Tyr666Tyr |
S305 |
17 | BAA01g43960 | A01 | 29096941 | C | T | missense_variant | MODERATE | c.2224C>T|p.Arg742Cys |
S46 |
18 | BAA01g43960 | A01 | 29097379 | C | T | intron_variant | MODIFIER | c.2344-10C>T| |
S58 |
19 | BAA01g43960 | A01 | 29098115 | G | A | missense_variant | MODERATE | c.2792G>A|p.Gly931Glu |
S243 S299 |
20 | BAA01g43960 | A01 | 29098461 | C | T | missense_variant | MODERATE | c.2902C>T|p.His968Tyr |
S279 |
21 | BAA01g43960 | A01 | 29099234 | C | T | missense_variant | MODERATE | c.3349C>T|p.Leu1117Phe |
S97 |