Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g03630 | A05 | 1825080 | A | G | upstream_gene_variant | MODIFIER | c.-4119A>G| |
S6 |
2 | BAA05g03630 | A05 | 1826476 | C | T | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S15 S3 |
3 | BAA05g03630 | A05 | 1827687 | C | T | upstream_gene_variant | MODIFIER | c.-1512C>T| |
S156 S2 |
4 | BAA05g03630 | A05 | 1828333 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S28 |
5 | BAA05g03630 | A05 | 1828984 | G | A | upstream_gene_variant | MODIFIER | c.-215G>A| |
S46 |
6 | BAA05g03630 | A05 | 1829101 | C | T | upstream_gene_variant | MODIFIER | c.-98C>T| |
S155 S211 |
7 | BAA05g03630 | A05 | 1829177 | G | A | upstream_gene_variant | MODIFIER | c.-22G>A| |
S112 |
8 | BAA05g03630 | A05 | 1829580 | C | T | missense_variant | MODERATE | c.382C>T|p.Pro128Ser |
S17 |
9 | BAA05g03630 | A05 | 1829598 | C | T | missense_variant | MODERATE | c.400C>T|p.Pro134Ser |
S251 |
10 | BAA05g03630 | A05 | 1829646 | C | T | missense_variant | MODERATE | c.448C>T|p.Pro150Ser |
S13 |
11 | BAA05g03630 | A05 | 1829820 | C | T | missense_variant | MODERATE | c.622C>T|p.Pro208Ser |
S10 |
12 | BAA05g03630 | A05 | 1830793 | G | A | synonymous_variant | LOW | c.1245G>A|p.Val415Val |
S23 |
13 | BAA05g03630 | A05 | 1830871 | G | A | synonymous_variant | LOW | c.1323G>A|p.Lys441Lys |
S293 |
14 | BAA05g03630 | A05 | 1831235 | C | T | missense_variant | MODERATE | c.1687C>T|p.Pro563Ser |
S82 S92 |
15 | BAA05g03630 | A05 | 1831350 | C | T | missense_variant | MODERATE | c.1802C>T|p.Pro601Leu |
S60 |
16 | BAA05g03630 | A05 | 1831478 | C | T | missense_variant | MODERATE | c.1930C>T|p.Pro644Ser |
S13 |
17 | BAA05g03630 | A05 | 1831640 | C | T | missense_variant | MODERATE | c.2092C>T|p.Pro698Ser |
S297 |
18 | BAA05g03630 | A05 | 1832457 | C | T | missense_variant | MODERATE | c.2909C>T|p.Pro970Leu |
S308 |
19 | BAA05g03630 | A05 | 1832562 | C | T | missense_variant | MODERATE | c.3014C>T|p.Ser1005Phe |
S28 |
20 | BAA05g03630 | A05 | 1832706 | C | T | missense_variant | MODERATE | c.3158C>T|p.Ser1053Phe |
S60 |