Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16590 | A05 | 9250147 | G | A | upstream_gene_variant | MODIFIER | c.-4246G>A| |
S64 |
2 | BAA05g16590 | A05 | 9250589 | G | A | upstream_gene_variant | MODIFIER | c.-3804G>A| |
S192 |
3 | BAA05g16590 | A05 | 9256725 | C | T | missense_variant | MODERATE | c.659C>T|p.Ala220Val |
S155 |
4 | BAA05g16590 | A05 | 9256810 | G | A | synonymous_variant | LOW | c.744G>A|p.Gly248Gly |
S152 |
5 | BAA05g16590 | A05 | 9257601 | G | A | missense_variant | MODERATE | c.1535G>A|p.Arg512His |
S226 |
6 | BAA05g16590 | A05 | 9257815 | G | A | synonymous_variant | LOW | c.1749G>A|p.Gln583Gln |
S56 |
7 | BAA05g16590 | A05 | 9257880 | G | A | missense_variant | MODERATE | c.1814G>A|p.Arg605Lys |
S173 |
8 | BAA05g16590 | A05 | 9258093 | C | T | missense_variant | MODERATE | c.2027C>T|p.Pro676Leu |
S273 |
9 | BAA05g16590 | A05 | 9258357 | G | A | missense_variant | MODERATE | c.2291G>A|p.Gly764Asp |
S176 |
10 | BAA05g16590 | A05 | 9258429 | G | A | intron_variant | MODIFIER | c.2351+12G>A| |
S70 |
11 | BAA05g16590 | A05 | 9258435 | C | T | intron_variant | MODIFIER | c.2351+18C>T| |
S136 |
12 | BAA05g16590 | A05 | 9258740 | C | T | missense_variant | MODERATE | c.2596C>T|p.Leu866Phe |
S72 S78 |
13 | BAA05g16590 | A05 | 9258932 | C | T | missense_variant | MODERATE | c.2788C>T|p.Arg930Cys |
S9 |
14 | BAA05g16590 | A05 | 9259405 | C | T | synonymous_variant | LOW | c.3261C>T|p.Asp1087Asp |
S162 |
15 | BAA05g16590 | A05 | 9259545 | G | A | missense_variant | MODERATE | c.3401G>A|p.Gly1134Glu |
S23 |
16 | BAA05g16590 | A05 | 9260810 | G | A | missense_variant | MODERATE | c.3517G>A|p.Asp1173Asn |
S70 |
17 | BAA05g16590 | A05 | 9260920 | G | A | synonymous_variant | LOW | c.3627G>A|p.Ser1209Ser |
S129 |
18 | BAA05g16590 | A05 | 9260986 | G | A | synonymous_variant | LOW | c.3693G>A|p.Arg1231Arg |
S40 S49 |
19 | BAA05g16590 | A05 | 9263539 | G | A | downstream_gene_variant | MODIFIER | c.*1414G>A| |
S282 |
20 | BAA05g16590 | A05 | 9264574 | C | T | downstream_gene_variant | MODIFIER | c.*2449C>T| |
S184 |