Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g05500 | A05 | 2684333 | C | T | missense_variant | MODERATE | c.8291G>A|p.Gly2764Glu |
S28 |
2 | BAA05g05500 | A05 | 2687663 | G | A | intron_variant | MODIFIER | c.6364-26C>T| |
S75 S81 |
3 | BAA05g05500 | A05 | 2688764 | C | T | missense_variant | MODERATE | c.5608G>A|p.Ala1870Thr |
S82 S92 |
4 | BAA05g05500 | A05 | 2689509 | G | A | missense_variant | MODERATE | c.5029C>T|p.Leu1677Phe |
S1 S90 |
5 | BAA05g05500 | A05 | 2690657 | C | T | synonymous_variant | LOW | c.4365G>A|p.Glu1455Glu |
S263 |
6 | BAA05g05500 | A05 | 2691058 | G | A | synonymous_variant | LOW | c.4146C>T|p.Ser1382Ser |
S241 S265 S39 |
7 | BAA05g05500 | A05 | 2693764 | C | T | missense_variant | MODERATE | c.2774G>A|p.Arg925Lys |
S2 |
8 | BAA05g05500 | A05 | 2694369 | C | T | synonymous_variant | LOW | c.2382G>A|p.Leu794Leu |
S245 |
9 | BAA05g05500 | A05 | 2694461 | C | T | missense_variant | MODERATE | c.2290G>A|p.Glu764Lys |
S241 |
10 | BAA05g05500 | A05 | 2695814 | C | T | missense_variant | MODERATE | c.1273G>A|p.Ala425Thr |
S283 |
11 | BAA05g05500 | A05 | 2696558 | C | T | missense_variant | MODERATE | c.529G>A|p.Val177Ile |
S71 |
12 | BAA05g05500 | A05 | 2696801 | C | T | missense_variant | MODERATE | c.286G>A|p.Asp96Asn |
S4 |
13 | BAA05g05500 | A05 | 2697582 | G | A | upstream_gene_variant | MODIFIER | c.-496C>T| |
S266 |
14 | BAA05g05500 | A05 | 2698729 | C | T | upstream_gene_variant | MODIFIER | c.-1643G>A| |
S180 |
15 | BAA05g05500 | A05 | 2699410 | C | T | upstream_gene_variant | MODIFIER | c.-2324G>A| |
S229 |
16 | BAA05g05500 | A05 | 2699593 | G | A | upstream_gene_variant | MODIFIER | c.-2507C>T| |
S126 |
17 | BAA05g05500 | A05 | 2700161 | C | T | upstream_gene_variant | MODIFIER | c.-3075G>A| |
S33 |
18 | BAA05g05500 | A05 | 2701935 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S132 S89 |