Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00540 | A04 | 326163 | C | T | synonymous_variant | LOW | c.5106G>A|p.Ser1702Ser |
S296 |
2 | BAA04g00540 | A04 | 326412 | G | A | synonymous_variant | LOW | c.4857C>T|p.Tyr1619Tyr |
S166 |
3 | BAA04g00540 | A04 | 326524 | A | C | missense_variant | MODERATE | c.4745T>G|p.Leu1582Arg |
S205 |
4 | BAA04g00540 | A04 | 326725 | G | A | missense_variant | MODERATE | c.4544C>T|p.Ser1515Phe |
S94 |
5 | BAA04g00540 | A04 | 328277 | C | T | missense_variant | MODERATE | c.2992G>A|p.Val998Ile |
S271 |
6 | BAA04g00540 | A04 | 328338 | G | A | synonymous_variant | LOW | c.2931C>T|p.Ile977Ile |
S303 |
7 | BAA04g00540 | A04 | 329056 | G | A | missense_variant | MODERATE | c.2213C>T|p.Ser738Phe |
S151 |
8 | BAA04g00540 | A04 | 329434 | C | T | missense_variant | MODERATE | c.1835G>A|p.Gly612Glu |
S289 S290 |
9 | BAA04g00540 | A04 | 329928 | G | A | missense_variant | MODERATE | c.1511C>T|p.Ser504Phe |
S282 |
10 | BAA04g00540 | A04 | 329943 | G | A | missense_variant | MODERATE | c.1496C>T|p.Ser499Phe |
S167 |
11 | BAA04g00540 | A04 | 330054 | G | A | missense_variant | MODERATE | c.1385C>T|p.Pro462Leu |
S77 S82 |
12 | BAA04g00540 | A04 | 330248 | G | A | synonymous_variant | LOW | c.1191C>T|p.Leu397Leu |
S62 |
13 | BAA04g00540 | A04 | 330275 | G | A | synonymous_variant | LOW | c.1164C>T|p.Leu388Leu |
S105 S106 |
14 | BAA04g00540 | A04 | 330603 | C | T | missense_variant | MODERATE | c.836G>A|p.Ser279Asn |
S187 |
15 | BAA04g00540 | A04 | 330917 | G | A | synonymous_variant | LOW | c.522C>T|p.Asp174Asp |
S282 |
16 | BAA04g00540 | A04 | 331176 | G | A | missense_variant | MODERATE | c.263C>T|p.Ser88Phe |
S150 |
17 | BAA04g00540 | A04 | 331658 | C | T | upstream_gene_variant | MODIFIER | c.-220G>A| |
S118 |
18 | BAA04g00540 | A04 | 333479 | G | A | upstream_gene_variant | MODIFIER | c.-2041C>T| |
S25 |
19 | BAA04g00540 | A04 | 335145 | C | T | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S44 |
20 | BAA04g00540 | A04 | 335893 | C | T | upstream_gene_variant | MODIFIER | c.-4455G>A| |
S158 |
21 | BAA04g00540 | A04 | 336167 | G | A | upstream_gene_variant | MODIFIER | c.-4729C>T| |
S103 S43 |