Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02380 | A06 | 1443520 | C | T | upstream_gene_variant | MODIFIER | c.-69C>T| |
S15 S3 |
2 | BAA06g02380 | A06 | 1443575 | G | T | upstream_gene_variant | MODIFIER | c.-14G>T| |
S64 |
3 | BAA06g02380 | A06 | 1444677 | C | T | intron_variant | MODIFIER | c.709-48C>T| |
S42 |
4 | BAA06g02380 | A06 | 1445101 | G | A | missense_variant | MODERATE | c.1085G>A|p.Gly362Asp |
S208 |
5 | BAA06g02380 | A06 | 1445311 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Phe |
S10 |
6 | BAA06g02380 | A06 | 1445522 | C | T | intron_variant | MODIFIER | c.1443+63C>T| |
S109 |
7 | BAA06g02380 | A06 | 1445867 | G | A | intron_variant | MODIFIER | c.1444-219G>A| |
S144 |
8 | BAA06g02380 | A06 | 1446052 | C | T | intron_variant | MODIFIER | c.1444-34C>T| |
S240 |
9 | BAA06g02380 | A06 | 1446662 | C | T | missense_variant | MODERATE | c.2020C>T|p.His674Tyr |
S46 |
10 | BAA06g02380 | A06 | 1446780 | G | A | missense_variant | MODERATE | c.2138G>A|p.Gly713Asp |
S298 |
11 | BAA06g02380 | A06 | 1448300 | C | T | downstream_gene_variant | MODIFIER | c.*1279C>T| |
S167 |
12 | BAA06g02380 | A06 | 1449445 | C | T | downstream_gene_variant | MODIFIER | c.*2424C>T| |
S225 S73 |