Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21770 | A09 | 13584769 | G | A | downstream_gene_variant | MODIFIER | c.*1293C>T| |
S266 |
2 | BAA09g21770 | A09 | 13585157 | G | A | downstream_gene_variant | MODIFIER | c.*905C>T| |
S247 |
3 | BAA09g21770 | A09 | 13585555 | C | T | downstream_gene_variant | MODIFIER | c.*507G>A| |
S255 |
4 | BAA09g21770 | A09 | 13586093 | G | A | missense_variant | MODERATE | c.5252C>T|p.Ala1751Val |
S191 S203 |
5 | BAA09g21770 | A09 | 13586097 | C | A | stop_gained | HIGH | c.5248G>T|p.Gly1750* |
S190 S286 |
6 | BAA09g21770 | A09 | 13586412 | G | A | missense_variant | MODERATE | c.5066C>T|p.Pro1689Leu |
S183 S198 |
7 | BAA09g21770 | A09 | 13586449 | C | T | missense_variant | MODERATE | c.5029G>A|p.Glu1677Lys |
S219 S72 |
8 | BAA09g21770 | A09 | 13587507 | C | T | missense_variant | MODERATE | c.4057G>A|p.Val1353Ile |
S87 |
9 | BAA09g21770 | A09 | 13587862 | G | A | synonymous_variant | LOW | c.3702C>T|p.Leu1234Leu |
S288 |
10 | BAA09g21770 | A09 | 13588121 | C | T | missense_variant | MODERATE | c.3443G>A|p.Arg1148Lys |
S260 |
11 | BAA09g21770 | A09 | 13588242 | G | A | stop_gained | HIGH | c.3322C>T|p.Gln1108* |
S72 S78 |
12 | BAA09g21770 | A09 | 13588696 | C | T | synonymous_variant | LOW | c.2868G>A|p.Gln956Gln |
S278 |
13 | BAA09g21770 | A09 | 13589321 | G | A | stop_gained | HIGH | c.2554C>T|p.Gln852* |
S162 |
14 | BAA09g21770 | A09 | 13590046 | C | T | stop_gained | HIGH | c.1829G>A|p.Trp610* |
S18 |
15 | BAA09g21770 | A09 | 13590111 | C | T | synonymous_variant | LOW | c.1764G>A|p.Lys588Lys |
S19 |
16 | BAA09g21770 | A09 | 13590336 | C | T | intron_variant | MODIFIER | c.1604-65G>A| |
S206 S26 |
17 | BAA09g21770 | A09 | 13590530 | C | T | intron_variant | MODIFIER | c.1604-259G>A| |
S273 |
18 | BAA09g21770 | A09 | 13590666 | C | T | intron_variant | MODIFIER | c.1604-395G>A| |
S263 |
19 | BAA09g21770 | A09 | 13592442 | C | T | synonymous_variant | LOW | c.1356G>A|p.Arg452Arg |
S103 |
20 | BAA09g21770 | A09 | 13593007 | G | A | missense_variant | MODERATE | c.791C>T|p.Thr264Ile |
S162 |
21 | BAA09g21770 | A09 | 13593699 | G | A | synonymous_variant | LOW | c.273C>T|p.Phe91Phe |
S182 |
22 | BAA09g21770 | A09 | 13597527 | G | A | upstream_gene_variant | MODIFIER | c.-3556C>T| |
S252 |
23 | BAA09g21770 | A09 | 13598420 | C | T | upstream_gene_variant | MODIFIER | c.-4449G>A| |
S36 |