Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06630 | A08 | 5421432 | G | A | upstream_gene_variant | MODIFIER | c.-4423G>A| |
S75 S81 |
2 | BAA08g06630 | A08 | 5421895 | G | A | upstream_gene_variant | MODIFIER | c.-3960G>A| |
S297 |
3 | BAA08g06630 | A08 | 5422283 | G | A | upstream_gene_variant | MODIFIER | c.-3572G>A| |
S204 |
4 | BAA08g06630 | A08 | 5424425 | G | A | upstream_gene_variant | MODIFIER | c.-1430G>A| |
S9 |
5 | BAA08g06630 | A08 | 5425489 | C | T | upstream_gene_variant | MODIFIER | c.-366C>T| |
S219 S72 |
6 | BAA08g06630 | A08 | 5425511 | G | A | upstream_gene_variant | MODIFIER | c.-344G>A| |
S103 |
7 | BAA08g06630 | A08 | 5425528 | C | T | upstream_gene_variant | MODIFIER | c.-327C>T| |
S201 |
8 | BAA08g06630 | A08 | 5426012 | C | T | missense_variant | MODERATE | c.158C>T|p.Pro53Leu |
S156 |
9 | BAA08g06630 | A08 | 5426979 | C | T | missense_variant | MODERATE | c.847C>T|p.Arg283Trp |
S125 |
10 | BAA08g06630 | A08 | 5426997 | C | T | missense_variant | MODERATE | c.865C>T|p.His289Tyr |
S152 |
11 | BAA08g06630 | A08 | 5427015 | G | A | missense_variant | MODERATE | c.883G>A|p.Glu295Lys |
S35 |
12 | BAA08g06630 | A08 | 5427647 | G | A | missense_variant | MODERATE | c.1444G>A|p.Ala482Thr |
S185 |
13 | BAA08g06630 | A08 | 5428149 | C | T | missense_variant | MODERATE | c.1946C>T|p.Ser649Phe |
S104 S52 |
14 | BAA08g06630 | A08 | 5428500 | G | A | synonymous_variant | LOW | c.2136G>A|p.Ser712Ser |
S234 |
15 | BAA08g06630 | A08 | 5428545 | C | T | synonymous_variant | LOW | c.2181C>T|p.Phe727Phe |
S174 S216 S241 |
16 | BAA08g06630 | A08 | 5429440 | G | A | missense_variant | MODERATE | c.2704G>A|p.Ala902Thr |
S297 |
17 | BAA08g06630 | A08 | 5429552 | C | T | missense_variant | MODERATE | c.2816C>T|p.Ala939Val |
S245 |
18 | BAA08g06630 | A08 | 5429586 | C | T | synonymous_variant | LOW | c.2850C>T|p.Arg950Arg |
S135 |
19 | BAA08g06630 | A08 | 5429649 | C | T | synonymous_variant | LOW | c.2913C>T|p.Val971Val |
S99 |
20 | BAA08g06630 | A08 | 5430075 | C | T | synonymous_variant | LOW | c.2991C>T|p.Leu997Leu |
S23 |
21 | BAA08g06630 | A08 | 5430078 | C | T | synonymous_variant | LOW | c.2994C>T|p.Ile998Ile |
S175 |
22 | BAA08g06630 | A08 | 5430276 | G | A | stop_gained | HIGH | c.3192G>A|p.Trp1064* |
S281 |
23 | BAA08g06630 | A08 | 5430370 | C | T | missense_variant | MODERATE | c.3286C>T|p.Pro1096Ser |
S294 |