Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06440 | A01 | 2864050 | G | A | synonymous_variant | LOW | c.4152C>T|p.Asn1384Asn |
S294 |
2 | BAA01g06440 | A01 | 2864827 | C | T | synonymous_variant | LOW | c.3756G>A|p.Lys1252Lys |
S218 |
3 | BAA01g06440 | A01 | 2865186 | C | T | intron_variant | MODIFIER | c.3519-31G>A| |
S68 |
4 | BAA01g06440 | A01 | 2865648 | G | A | intron_variant | MODIFIER | c.3285+22C>T| |
S251 |
5 | BAA01g06440 | A01 | 2865690 | G | A | stop_gained | HIGH | c.3265C>T|p.Arg1089* |
S298 |
6 | BAA01g06440 | A01 | 2865799 | G | A | intron_variant | MODIFIER | c.3219-63C>T| |
S284 |
7 | BAA01g06440 | A01 | 2865925 | G | A | intron_variant | MODIFIER | c.3218+12C>T| |
S57 |
8 | BAA01g06440 | A01 | 2866119 | G | A | intron_variant | MODIFIER | c.3049-13C>T| |
S116 |
9 | BAA01g06440 | A01 | 2866204 | C | T | intron_variant | MODIFIER | c.3048+11G>A| |
S130 |
10 | BAA01g06440 | A01 | 2866733 | G | A | missense_variant | MODERATE | c.2716C>T|p.Leu906Phe |
S28 |
11 | BAA01g06440 | A01 | 2866872 | G | A | missense_variant | MODERATE | c.2665C>T|p.Leu889Phe |
S142 |
12 | BAA01g06440 | A01 | 2868383 | C | T | intron_variant | MODIFIER | c.1981+28G>A| |
S148 S210 S30 S31 |
13 | BAA01g06440 | A01 | 2868966 | C | T | intron_variant | MODIFIER | c.1604+50G>A| |
S132 S137 S215 S89 |
14 | BAA01g06440 | A01 | 2869128 | G | A | missense_variant | MODERATE | c.1492C>T|p.Arg498Cys |
S219 |
15 | BAA01g06440 | A01 | 2869438 | G | A | intron_variant | MODIFIER | c.1447-265C>T| |
S199 |
16 | BAA01g06440 | A01 | 2869721 | C | T | intron_variant | MODIFIER | c.1447-548G>A| |
S130 |
17 | BAA01g06440 | A01 | 2870728 | C | T | intron_variant | MODIFIER | c.1446+1023G>A| |
S100 |
18 | BAA01g06440 | A01 | 2871134 | C | T | intron_variant | MODIFIER | c.1446+617G>A| |
S153 S213 |
19 | BAA01g06440 | A01 | 2871151 | G | A | intron_variant | MODIFIER | c.1446+600C>T| |
S129 |
20 | BAA01g06440 | A01 | 2871295 | G | A | intron_variant | MODIFIER | c.1446+456C>T| |
S209 |
21 | BAA01g06440 | A01 | 2871342 | C | T | intron_variant | MODIFIER | c.1446+409G>A| |
S36 |
22 | BAA01g06440 | A01 | 2871453 | C | T | intron_variant | MODIFIER | c.1446+298G>A| |
S255 |
23 | BAA01g06440 | A01 | 2871496 | G | A | intron_variant | MODIFIER | c.1446+255C>T| |
S23 |
24 | BAA01g06440 | A01 | 2871540 | A | T | intron_variant | MODIFIER | c.1446+211T>A| |
S98 |
25 | BAA01g06440 | A01 | 2871603 | C | T | intron_variant | MODIFIER | c.1446+148G>A| |
S46 |