Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07830 | A10 | 4849313 | G | A | downstream_gene_variant | MODIFIER | c.*3575C>T| |
S268 |
2 | BAA10g07830 | A10 | 4853034 | G | A | missense_variant | MODERATE | c.1075C>T|p.Leu359Phe |
S198 |
3 | BAA10g07830 | A10 | 4853684 | G | A | stop_gained | HIGH | c.862C>T|p.Gln288* |
S226 |
4 | BAA10g07830 | A10 | 4854121 | C | T | missense_variant&splice_region_variant | MODERATE | c.577G>A|p.Val193Ile |
S19 |
5 | BAA10g07830 | A10 | 4854624 | G | A | missense_variant | MODERATE | c.374C>T|p.Thr125Met |
S17 |
6 | BAA10g07830 | A10 | 4854803 | C | T | missense_variant | MODERATE | c.284G>A|p.Arg95Lys |
S40 S49 |
7 | BAA10g07830 | A10 | 4855074 | G | A | missense_variant | MODERATE | c.83C>T|p.Ala28Val |
S32 |
8 | BAA10g07830 | A10 | 4857033 | C | T | upstream_gene_variant | MODIFIER | c.-1877G>A| |
S23 |
9 | BAA10g07830 | A10 | 4857749 | C | T | upstream_gene_variant | MODIFIER | c.-2593G>A| |
S54 |
10 | BAA10g07830 | A10 | 4859330 | C | T | upstream_gene_variant | MODIFIER | c.-4174G>A| |
S84 S93 |
11 | BAA10g07830 | A10 | 4859409 | C | T | upstream_gene_variant | MODIFIER | c.-4253G>A| |
S235 |
12 | BAA10g07830 | A10 | 4859523 | C | T | upstream_gene_variant | MODIFIER | c.-4367G>A| |
S246 |