Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01530 | A04 | 895478 | C | T | synonymous_variant | LOW | c.2154G>A|p.Lys718Lys |
S140 |
2 | BAA04g01530 | A04 | 895537 | C | T | missense_variant | MODERATE | c.2095G>A|p.Gly699Arg |
S293 |
3 | BAA04g01530 | A04 | 895657 | C | T | missense_variant | MODERATE | c.1975G>A|p.Glu659Lys |
S255 |
4 | BAA04g01530 | A04 | 896001 | G | A | missense_variant | MODERATE | c.1631C>T|p.Thr544Ile |
S183 S198 |
5 | BAA04g01530 | A04 | 896150 | G | A | synonymous_variant | LOW | c.1482C>T|p.Leu494Leu |
S158 |
6 | BAA04g01530 | A04 | 896196 | C | T | missense_variant | MODERATE | c.1436G>A|p.Gly479Asp |
S256 |
7 | BAA04g01530 | A04 | 896283 | G | A | missense_variant | MODERATE | c.1349C>T|p.Ala450Val |
S126 |
8 | BAA04g01530 | A04 | 896294 | G | A | synonymous_variant | LOW | c.1338C>T|p.Leu446Leu |
S166 |
9 | BAA04g01530 | A04 | 896361 | C | T | missense_variant | MODERATE | c.1271G>A|p.Gly424Asp |
S184 |
10 | BAA04g01530 | A04 | 897507 | G | A | missense_variant | MODERATE | c.973C>T|p.Pro325Ser |
S305 |
11 | BAA04g01530 | A04 | 898065 | C | T | missense_variant | MODERATE | c.565G>A|p.Gly189Arg |
S289 S290 |
12 | BAA04g01530 | A04 | 898370 | G | A | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S120 |
13 | BAA04g01530 | A04 | 898461 | G | A | synonymous_variant | LOW | c.333C>T|p.Leu111Leu |
S167 |
14 | BAA04g01530 | A04 | 898736 | G | A | missense_variant | MODERATE | c.58C>T|p.Leu20Phe |
S5 |
15 | BAA04g01530 | A04 | 899619 | G | A | upstream_gene_variant | MODIFIER | c.-826C>T| |
S190 |
16 | BAA04g01530 | A04 | 901485 | G | A | upstream_gene_variant | MODIFIER | c.-2692C>T| |
S203 |
17 | BAA04g01530 | A04 | 903567 | G | A | upstream_gene_variant | MODIFIER | c.-4774C>T| |
S261 |
18 | BAA04g01530 | A04 | 903602 | C | T | upstream_gene_variant | MODIFIER | c.-4809G>A| |
S19 |