Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66660 | A03 | 41056202 | G | A | upstream_gene_variant | MODIFIER | c.-186G>A| |
S60 |
2 | BAA03g66660 | A03 | 41056266 | G | A | upstream_gene_variant | MODIFIER | c.-122G>A| |
S122 |
3 | BAA03g66660 | A03 | 41056648 | G | A | synonymous_variant | LOW | c.222G>A|p.Arg74Arg |
S114 |
4 | BAA03g66660 | A03 | 41056995 | C | T | synonymous_variant | LOW | c.459C>T|p.Asn153Asn |
S144 |
5 | BAA03g66660 | A03 | 41057072 | G | A | missense_variant | MODERATE | c.536G>A|p.Arg179Lys |
S130 |
6 | BAA03g66660 | A03 | 41057280 | C | T | synonymous_variant | LOW | c.744C>T|p.Ile248Ile |
S52 |
7 | BAA03g66660 | A03 | 41057765 | G | A | missense_variant | MODERATE | c.1229G>A|p.Gly410Glu |
S239 |
8 | BAA03g66660 | A03 | 41059996 | G | A | synonymous_variant | LOW | c.2010G>A|p.Leu670Leu |
S81 S85 |
9 | BAA03g66660 | A03 | 41060767 | G | A | missense_variant | MODERATE | c.2509G>A|p.Val837Ile |
S296 |
10 | BAA03g66660 | A03 | 41061578 | C | A | intron_variant | MODIFIER | c.3043+176C>A| |
S283 |
11 | BAA03g66660 | A03 | 41061650 | G | T | intron_variant | MODIFIER | c.3043+248G>T| |
S52 |
12 | BAA03g66660 | A03 | 41062209 | G | A | intron_variant | MODIFIER | c.3043+807G>A| |
S69 |
13 | BAA03g66660 | A03 | 41062317 | G | A | intron_variant | MODIFIER | c.3043+915G>A| |
S132 S137 S215 S89 |
14 | BAA03g66660 | A03 | 41062691 | C | T | intron_variant | MODIFIER | c.3043+1289C>T| |
S2 |
15 | BAA03g66660 | A03 | 41063418 | C | T | intron_variant | MODIFIER | c.3044-1781C>T| |
S126 |
16 | BAA03g66660 | A03 | 41064066 | G | A | intron_variant | MODIFIER | c.3044-1133G>A| |
S303 |
17 | BAA03g66660 | A03 | 41064086 | C | T | intron_variant | MODIFIER | c.3044-1113C>T| |
S45 |
18 | BAA03g66660 | A03 | 41064235 | G | A | intron_variant | MODIFIER | c.3044-964G>A| |
S36 |
19 | BAA03g66660 | A03 | 41064401 | G | A | intron_variant | MODIFIER | c.3044-798G>A| |
S230 |
20 | BAA03g66660 | A03 | 41064733 | C | T | intron_variant | MODIFIER | c.3044-466C>T| |
S281 |
21 | BAA03g66660 | A03 | 41065241 | C | A | missense_variant | MODERATE | c.3086C>A|p.Ser1029Tyr |
S240 |
22 | BAA03g66660 | A03 | 41065643 | C | T | downstream_gene_variant | MODIFIER | c.*163C>T| |
S100 |
23 | BAA03g66660 | A03 | 41065649 | C | A | downstream_gene_variant | MODIFIER | c.*169C>A| |
S211 S227 |
24 | BAA03g66660 | A03 | 41065771 | G | A | downstream_gene_variant | MODIFIER | c.*291G>A| |
S302 |
25 | BAA03g66660 | A03 | 41066176 | G | A | downstream_gene_variant | MODIFIER | c.*696G>A| |
S165 |