Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19670 | A10 | 17977905 | G | A | downstream_gene_variant | MODIFIER | c.*1355C>T| |
S298 |
2 | BAA10g19670 | A10 | 17978328 | G | A | downstream_gene_variant | MODIFIER | c.*932C>T| |
S207 |
3 | BAA10g19670 | A10 | 17978463 | C | T | downstream_gene_variant | MODIFIER | c.*797G>A| |
S187 |
4 | BAA10g19670 | A10 | 17978473 | C | T | downstream_gene_variant | MODIFIER | c.*787G>A| |
S202 |
5 | BAA10g19670 | A10 | 17978920 | G | A | downstream_gene_variant | MODIFIER | c.*340C>T| |
S76 |
6 | BAA10g19670 | A10 | 17978985 | C | T | downstream_gene_variant | MODIFIER | c.*275G>A| |
S125 |
7 | BAA10g19670 | A10 | 17979472 | C | T | missense_variant | MODERATE | c.1510G>A|p.Ala504Thr |
S202 |
8 | BAA10g19670 | A10 | 17979578 | G | A | synonymous_variant | LOW | c.1404C>T|p.Leu468Leu |
S176 |
9 | BAA10g19670 | A10 | 17979705 | G | A | missense_variant | MODERATE | c.1277C>T|p.Pro426Leu |
S59 |
10 | BAA10g19670 | A10 | 17979804 | G | A | missense_variant | MODERATE | c.1178C>T|p.Thr393Met |
S38 |
11 | BAA10g19670 | A10 | 17979965 | G | A | synonymous_variant | LOW | c.1017C>T|p.Tyr339Tyr |
S67 |
12 | BAA10g19670 | A10 | 17980104 | C | T | missense_variant | MODERATE | c.878G>A|p.Arg293Lys |
S92 |
13 | BAA10g19670 | A10 | 17980117 | G | A | missense_variant | MODERATE | c.865C>T|p.Pro289Ser |
S71 |
14 | BAA10g19670 | A10 | 17980140 | G | A | missense_variant | MODERATE | c.842C>T|p.Ser281Phe |
S94 |
15 | BAA10g19670 | A10 | 17980954 | C | T | missense_variant | MODERATE | c.545G>A|p.Gly182Glu |
S297 |
16 | BAA10g19670 | A10 | 17982224 | C | T | upstream_gene_variant | MODIFIER | c.-555G>A| |
S242 |
17 | BAA10g19670 | A10 | 17985121 | G | A | upstream_gene_variant | MODIFIER | c.-3452C>T| |
S286 |
18 | BAA10g19670 | A10 | 17985907 | G | A | upstream_gene_variant | MODIFIER | c.-4238C>T| |
S181 |