Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g04250 | A06 | 2369577 | G | A | upstream_gene_variant | MODIFIER | c.-4211G>A| |
S233 |
2 | BAA06g04250 | A06 | 2370321 | G | A | upstream_gene_variant | MODIFIER | c.-3467G>A| |
S15 S3 |
3 | BAA06g04250 | A06 | 2370392 | G | A | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S143 |
4 | BAA06g04250 | A06 | 2370755 | C | T | upstream_gene_variant | MODIFIER | c.-3033C>T| |
S10 |
5 | BAA06g04250 | A06 | 2371411 | C | T | upstream_gene_variant | MODIFIER | c.-2377C>T| |
S63 |
6 | BAA06g04250 | A06 | 2371447 | C | T | upstream_gene_variant | MODIFIER | c.-2341C>T| |
S183 S198 |
7 | BAA06g04250 | A06 | 2372955 | G | A | upstream_gene_variant | MODIFIER | c.-833G>A| |
S60 |
8 | BAA06g04250 | A06 | 2374057 | G | A | missense_variant | MODERATE | c.169G>A|p.Gly57Ser |
S261 |
9 | BAA06g04250 | A06 | 2374953 | C | T | missense_variant | MODERATE | c.527C>T|p.Thr176Met |
S112 |
10 | BAA06g04250 | A06 | 2375871 | C | T | missense_variant | MODERATE | c.1445C>T|p.Ala482Val |
S192 |
11 | BAA06g04250 | A06 | 2375902 | C | T | synonymous_variant | LOW | c.1476C>T|p.His492His |
S18 |
12 | BAA06g04250 | A06 | 2377191 | C | T | downstream_gene_variant | MODIFIER | c.*47C>T| |
S111 |
13 | BAA06g04250 | A06 | 2377702 | C | T | downstream_gene_variant | MODIFIER | c.*558C>T| |
S192 |