Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g21220 | A05 | 13465021 | C | T | upstream_gene_variant | MODIFIER | c.-4220C>T| |
S121 |
2 | BAA05g21220 | A05 | 13466770 | C | T | upstream_gene_variant | MODIFIER | c.-2471C>T| |
S167 |
3 | BAA05g21220 | A05 | 13467689 | G | A | upstream_gene_variant | MODIFIER | c.-1552G>A| |
S125 |
4 | BAA05g21220 | A05 | 13467691 | G | A | upstream_gene_variant | MODIFIER | c.-1550G>A| |
S41 |
5 | BAA05g21220 | A05 | 13468196 | C | T | upstream_gene_variant | MODIFIER | c.-1045C>T| |
S140 |
6 | BAA05g21220 | A05 | 13468549 | G | A | upstream_gene_variant | MODIFIER | c.-692G>A| |
S252 |
7 | BAA05g21220 | A05 | 13468866 | G | A | upstream_gene_variant | MODIFIER | c.-375G>A| |
S266 |
8 | BAA05g21220 | A05 | 13469337 | G | A | missense_variant | MODERATE | c.97G>A|p.Val33Ile |
S294 |
9 | BAA05g21220 | A05 | 13470228 | C | T | missense_variant | MODERATE | c.287C>T|p.Ser96Phe |
S67 |
10 | BAA05g21220 | A05 | 13470301 | G | A | stop_gained | HIGH | c.360G>A|p.Trp120* |
S173 |
11 | BAA05g21220 | A05 | 13470481 | C | T | missense_variant | MODERATE | c.461C>T|p.Ser154Phe |
S241 |
12 | BAA05g21220 | A05 | 13470544 | C | T | missense_variant | MODERATE | c.524C>T|p.Ala175Val |
S18 |
13 | BAA05g21220 | A05 | 13470769 | C | T | missense_variant | MODERATE | c.662C>T|p.Ser221Phe |
S203 |
14 | BAA05g21220 | A05 | 13471229 | G | A | missense_variant | MODERATE | c.928G>A|p.Val310Ile |
S244 |
15 | BAA05g21220 | A05 | 13471278 | G | A | splice_region_variant&intron_variant | LOW | c.974+3G>A| |
S66 |
16 | BAA05g21220 | A05 | 13471904 | G | A | missense_variant | MODERATE | c.1345G>A|p.Ala449Thr |
S15 |
17 | BAA05g21220 | A05 | 13471988 | G | A | missense_variant | MODERATE | c.1429G>A|p.Val477Ile |
S280 |
18 | BAA05g21220 | A05 | 13472163 | C | T | downstream_gene_variant | MODIFIER | c.*155C>T| |
S156 S2 S213 S3 S34 S4 S6 |