Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08120 | A04 | 5531179 | C | T | downstream_gene_variant | MODIFIER | c.*4343G>A| |
S25 S264 |
2 | BAA04g08120 | A04 | 5534338 | G | A | downstream_gene_variant | MODIFIER | c.*1184C>T| |
S87 |
3 | BAA04g08120 | A04 | 5534368 | G | A | downstream_gene_variant | MODIFIER | c.*1154C>T| |
S79 S91 |
4 | BAA04g08120 | A04 | 5534370 | G | A | downstream_gene_variant | MODIFIER | c.*1152C>T| |
S65 |
5 | BAA04g08120 | A04 | 5534427 | G | A | downstream_gene_variant | MODIFIER | c.*1095C>T| |
S236 |
6 | BAA04g08120 | A04 | 5534622 | C | T | downstream_gene_variant | MODIFIER | c.*900G>A| |
S111 |
7 | BAA04g08120 | A04 | 5534631 | C | T | downstream_gene_variant | MODIFIER | c.*891G>A| |
S48 |
8 | BAA04g08120 | A04 | 5534852 | G | A | downstream_gene_variant | MODIFIER | c.*670C>T| |
S277 |
9 | BAA04g08120 | A04 | 5535057 | C | T | downstream_gene_variant | MODIFIER | c.*465G>A| |
S263 |
10 | BAA04g08120 | A04 | 5535123 | G | A | downstream_gene_variant | MODIFIER | c.*399C>T| |
S85 |
11 | BAA04g08120 | A04 | 5535671 | C | T | missense_variant | MODERATE | c.4336G>A|p.Glu1446Lys |
S140 |
12 | BAA04g08120 | A04 | 5536559 | C | T | synonymous_variant | LOW | c.3663G>A|p.Leu1221Leu |
S294 |
13 | BAA04g08120 | A04 | 5537168 | G | A | splice_region_variant&intron_variant | LOW | c.3252+7C>T| |
S241 |
14 | BAA04g08120 | A04 | 5537652 | C | T | synonymous_variant | LOW | c.2928G>A|p.Gln976Gln |
S80 |
15 | BAA04g08120 | A04 | 5537809 | C | T | missense_variant | MODERATE | c.2842G>A|p.Glu948Lys |
S28 |
16 | BAA04g08120 | A04 | 5538345 | G | A | missense_variant | MODERATE | c.2306C>T|p.Ala769Val |
S262 |
17 | BAA04g08120 | A04 | 5538778 | G | A | stop_gained | HIGH | c.1957C>T|p.Gln653* |
S295 |
18 | BAA04g08120 | A04 | 5539563 | G | A | synonymous_variant | LOW | c.1309C>T|p.Leu437Leu |
S166 |
19 | BAA04g08120 | A04 | 5540158 | G | A | synonymous_variant | LOW | c.1230C>T|p.Asp410Asp |
S264 |
20 | BAA04g08120 | A04 | 5540733 | C | T | intron_variant | MODIFIER | c.851-115G>A| |
S247 |
21 | BAA04g08120 | A04 | 5540977 | G | A | intron_variant | MODIFIER | c.850+90C>T| |
S144 |
22 | BAA04g08120 | A04 | 5541528 | C | T | missense_variant | MODERATE | c.389G>A|p.Gly130Glu |
S295 |
23 | BAA04g08120 | A04 | 5541662 | C | T | synonymous_variant | LOW | c.255G>A|p.Ala85Ala |
S202 |
24 | BAA04g08120 | A04 | 5541801 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S232 |
25 | BAA04g08120 | A04 | 5541828 | G | A | missense_variant | MODERATE | c.89C>T|p.Pro30Leu |
S186 S275 |