Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18830 | A09 | 11330157 | G | A | missense_variant | MODERATE | c.2203G>A|p.Asp735Asn |
S7 |
2 | BAA09g18830 | A09 | 11330432 | T | G | synonymous_variant | LOW | c.2478T>G|p.Leu826Leu |
S297 |
3 | BAA09g18830 | A09 | 11330816 | G | A | synonymous_variant | LOW | c.2862G>A|p.Thr954Thr |
S1 S90 |
4 | BAA09g18830 | A09 | 11331250 | G | A | missense_variant | MODERATE | c.3296G>A|p.Arg1099Lys |
S259 |
5 | BAA09g18830 | A09 | 11331409 | A | T | missense_variant | MODERATE | c.3455A>T|p.Asp1152Val |
S207 |
6 | BAA09g18830 | A09 | 11332728 | G | A | missense_variant | MODERATE | c.4774G>A|p.Asp1592Asn |
S196 |
7 | BAA09g18830 | A09 | 11332847 | G | A | synonymous_variant | LOW | c.4893G>A|p.Gln1631Gln |
S86 |
8 | BAA09g18830 | A09 | 11333158 | C | T | missense_variant | MODERATE | c.5204C>T|p.Ser1735Phe |
S242 |
9 | BAA09g18830 | A09 | 11333306 | C | T | synonymous_variant | LOW | c.5352C>T|p.Gly1784Gly |
S270 |
10 | BAA09g18830 | A09 | 11334418 | C | T | missense_variant | MODERATE | c.6464C>T|p.Thr2155Ile |
S255 |
11 | BAA09g18830 | A09 | 11334892 | G | A | synonymous_variant | LOW | c.6801G>A|p.Gln2267Gln |
S260 |
12 | BAA09g18830 | A09 | 11335304 | G | A | missense_variant | MODERATE | c.7213G>A|p.Val2405Met |
S172 S217 |
13 | BAA09g18830 | A09 | 11335479 | C | T | missense_variant | MODERATE | c.7388C>T|p.Ala2463Val |
S164 |
14 | BAA09g18830 | A09 | 11336529 | C | T | synonymous_variant | LOW | c.8200C>T|p.Leu2734Leu |
S63 |
15 | BAA09g18830 | A09 | 11336549 | C | T | synonymous_variant | LOW | c.8220C>T|p.Ser2740Ser |
S297 |
16 | BAA09g18830 | A09 | 11336837 | C | T | synonymous_variant | LOW | c.8415C>T|p.Val2805Val |
S250 |
17 | BAA09g18830 | A09 | 11337300 | G | A | missense_variant | MODERATE | c.8759G>A|p.Cys2920Tyr |
S198 |
18 | BAA09g18830 | A09 | 11338453 | G | A | missense_variant | MODERATE | c.9814G>A|p.Gly3272Ser |
S267 |