Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02210 | A04 | 1294425 | G | A | upstream_gene_variant | MODIFIER | c.-4311G>A| |
S275 |
2 | BAA04g02210 | A04 | 1295535 | G | A | upstream_gene_variant | MODIFIER | c.-3201G>A| |
S5 |
3 | BAA04g02210 | A04 | 1295759 | C | T | upstream_gene_variant | MODIFIER | c.-2977C>T| |
S184 |
4 | BAA04g02210 | A04 | 1295796 | G | A | upstream_gene_variant | MODIFIER | c.-2940G>A| |
S244 |
5 | BAA04g02210 | A04 | 1297743 | G | A | upstream_gene_variant | MODIFIER | c.-993G>A| |
S246 |
6 | BAA04g02210 | A04 | 1297811 | C | T | upstream_gene_variant | MODIFIER | c.-925C>T| |
S169 |
7 | BAA04g02210 | A04 | 1297846 | G | A | upstream_gene_variant | MODIFIER | c.-890G>A| |
S207 |
8 | BAA04g02210 | A04 | 1298229 | C | T | upstream_gene_variant | MODIFIER | c.-507C>T| |
S168 |
9 | BAA04g02210 | A04 | 1298971 | C | T | missense_variant | MODERATE | c.236C>T|p.Thr79Ile |
S202 |
10 | BAA04g02210 | A04 | 1299508 | C | T | missense_variant | MODERATE | c.773C>T|p.Ser258Phe |
S132 S137 S215 S89 |
11 | BAA04g02210 | A04 | 1299657 | G | A | missense_variant | MODERATE | c.922G>A|p.Ala308Thr |
S104 |
12 | BAA04g02210 | A04 | 1299709 | G | A | missense_variant | MODERATE | c.974G>A|p.Arg325Lys |
S234 |
13 | BAA04g02210 | A04 | 1299805 | G | A | missense_variant | MODERATE | c.1070G>A|p.Cys357Tyr |
S162 |
14 | BAA04g02210 | A04 | 1299904 | G | A | missense_variant | MODERATE | c.1169G>A|p.Cys390Tyr |
S108 |
15 | BAA04g02210 | A04 | 1300164 | G | A | missense_variant | MODERATE | c.1429G>A|p.Gly477Ser |
S282 |
16 | BAA04g02210 | A04 | 1300180 | C | T | missense_variant | MODERATE | c.1445C>T|p.Ser482Leu |
S116 |
17 | BAA04g02210 | A04 | 1300222 | C | T | missense_variant | MODERATE | c.1487C>T|p.Ser496Phe |
S134 |
18 | BAA04g02210 | A04 | 1300502 | C | T | intron_variant | MODIFIER | c.1727+40C>T| |
S297 |
19 | BAA04g02210 | A04 | 1301403 | G | A | missense_variant | MODERATE | c.2437G>A|p.Asp813Asn |
S219 |
20 | BAA04g02210 | A04 | 1301442 | G | A | missense_variant | MODERATE | c.2476G>A|p.Glu826Lys |
S33 |
21 | BAA04g02210 | A04 | 1301549 | G | A | synonymous_variant | LOW | c.2583G>A|p.Val861Val |
S232 |
22 | BAA04g02210 | A04 | 1301673 | G | A | missense_variant | MODERATE | c.2707G>A|p.Glu903Lys |
S167 |
23 | BAA04g02210 | A04 | 1302012 | C | T | synonymous_variant | LOW | c.3046C>T|p.Leu1016Leu |
S1 |
24 | BAA04g02210 | A04 | 1304717 | G | A | downstream_gene_variant | MODIFIER | c.*429G>A| |
S236 |
25 | BAA04g02210 | A04 | 1305541 | G | A | downstream_gene_variant | MODIFIER | c.*1253G>A| |
S167 S251 |