Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28220 | A01 | 17267970 | G | A | downstream_gene_variant | MODIFIER | c.*4262C>T| |
S74 |
2 | BAA01g28220 | A01 | 17268020 | C | T | downstream_gene_variant | MODIFIER | c.*4212G>A| |
S266 |
3 | BAA01g28220 | A01 | 17268025 | G | A | downstream_gene_variant | MODIFIER | c.*4207C>T| |
S197 |
4 | BAA01g28220 | A01 | 17268051 | G | A | downstream_gene_variant | MODIFIER | c.*4181C>T| |
S262 |
5 | BAA01g28220 | A01 | 17268381 | C | T | downstream_gene_variant | MODIFIER | c.*3851G>A| |
S256 |
6 | BAA01g28220 | A01 | 17269585 | G | A | downstream_gene_variant | MODIFIER | c.*2647C>T| |
S298 |
7 | BAA01g28220 | A01 | 17269666 | C | T | downstream_gene_variant | MODIFIER | c.*2566G>A| |
S146 |
8 | BAA01g28220 | A01 | 17269754 | C | T | downstream_gene_variant | MODIFIER | c.*2478G>A| |
S18 |
9 | BAA01g28220 | A01 | 17270422 | G | A | downstream_gene_variant | MODIFIER | c.*1810C>T| |
S241 |
10 | BAA01g28220 | A01 | 17271017 | C | T | downstream_gene_variant | MODIFIER | c.*1215G>A| |
S18 |
11 | BAA01g28220 | A01 | 17271547 | C | T | downstream_gene_variant | MODIFIER | c.*685G>A| |
S146 |
12 | BAA01g28220 | A01 | 17271782 | G | A | downstream_gene_variant | MODIFIER | c.*450C>T| |
S94 |
13 | BAA01g28220 | A01 | 17271985 | C | T | downstream_gene_variant | MODIFIER | c.*247G>A| |
S297 |
14 | BAA01g28220 | A01 | 17272278 | G | A | missense_variant | MODERATE | c.1304C>T|p.Ala435Val |
S58 |
15 | BAA01g28220 | A01 | 17273091 | C | T | synonymous_variant | LOW | c.825G>A|p.Lys275Lys |
S136 |
16 | BAA01g28220 | A01 | 17273279 | C | T | splice_donor_variant&intron_variant | HIGH | c.768+1G>A| |
S269 |
17 | BAA01g28220 | A01 | 17273329 | C | T | missense_variant | MODERATE | c.719G>A|p.Gly240Asp |
S77 |
18 | BAA01g28220 | A01 | 17273369 | C | T | missense_variant | MODERATE | c.679G>A|p.Gly227Arg |
S277 |
19 | BAA01g28220 | A01 | 17273382 | C | T | synonymous_variant | LOW | c.666G>A|p.Thr222Thr |
S249 |
20 | BAA01g28220 | A01 | 17273494 | C | T | splice_region_variant&intron_variant | LOW | c.559-5G>A| |
S59 |
21 | BAA01g28220 | A01 | 17274717 | G | A | upstream_gene_variant | MODIFIER | c.-246C>T| |
S265 |
22 | BAA01g28220 | A01 | 17274731 | C | T | upstream_gene_variant | MODIFIER | c.-260G>A| |
S20 |
23 | BAA01g28220 | A01 | 17275907 | G | A | upstream_gene_variant | MODIFIER | c.-1436C>T| |
S70 |
24 | BAA01g28220 | A01 | 17278102 | G | A | upstream_gene_variant | MODIFIER | c.-3631C>T| |
S265 |
25 | BAA01g28220 | A01 | 17278676 | C | T | upstream_gene_variant | MODIFIER | c.-4205G>A| |
S250 |