Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21090 | A06 | 11310561 | G | A | upstream_gene_variant | MODIFIER | c.-4908G>A| |
S81 |
2 | BAA06g21090 | A06 | 11310773 | G | A | upstream_gene_variant | MODIFIER | c.-4696G>A| |
S69 |
3 | BAA06g21090 | A06 | 11315633 | C | T | synonymous_variant | LOW | c.165C>T|p.Ser55Ser |
S37 |
4 | BAA06g21090 | A06 | 11315840 | G | A | synonymous_variant | LOW | c.372G>A|p.Gly124Gly |
S201 |
5 | BAA06g21090 | A06 | 11317255 | G | A | intron_variant | MODIFIER | c.1498-103G>A| |
S5 |
6 | BAA06g21090 | A06 | 11318239 | A | G | synonymous_variant | LOW | c.2379A>G|p.Ala793Ala |
S270 |
7 | BAA06g21090 | A06 | 11318543 | G | A | intron_variant | MODIFIER | c.2552+131G>A| |
S173 |
8 | BAA06g21090 | A06 | 11318750 | C | T | intron_variant | MODIFIER | c.2552+338C>T| |
S205 |
9 | BAA06g21090 | A06 | 11319754 | G | A | missense_variant | MODERATE | c.2943G>A|p.Met981Ile |
S179 |
10 | BAA06g21090 | A06 | 11319853 | C | T | synonymous_variant | LOW | c.3042C>T|p.Tyr1014Tyr |
S25 |
11 | BAA06g21090 | A06 | 11320630 | C | T | synonymous_variant | LOW | c.3819C>T|p.Val1273Val |
S14 |
12 | BAA06g21090 | A06 | 11320694 | C | T | stop_gained | HIGH | c.3883C>T|p.Arg1295* |
S135 |