Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41350 | A06 | 26901781 | G | A | downstream_gene_variant | MODIFIER | c.*3147C>T| |
S262 |
2 | BAA06g41350 | A06 | 26903491 | C | T | downstream_gene_variant | MODIFIER | c.*1437G>A| |
S172 S217 |
3 | BAA06g41350 | A06 | 26905151 | G | A | missense_variant | MODERATE | c.3506C>T|p.Thr1169Ile |
S23 |
4 | BAA06g41350 | A06 | 26905616 | G | A | stop_gained | HIGH | c.3124C>T|p.Gln1042* |
S146 |
5 | BAA06g41350 | A06 | 26906134 | G | A | synonymous_variant | LOW | c.2682C>T|p.Thr894Thr |
S79 |
6 | BAA06g41350 | A06 | 26906375 | G | A | missense_variant | MODERATE | c.2441C>T|p.Ser814Phe |
S170 |
7 | BAA06g41350 | A06 | 26906981 | C | T | missense_variant | MODERATE | c.2062G>A|p.Asp688Asn |
S132 S137 |
8 | BAA06g41350 | A06 | 26907086 | G | A | splice_region_variant&synonymous_variant | LOW | c.2044C>T|p.Leu682Leu |
S2 |
9 | BAA06g41350 | A06 | 26907765 | G | A | synonymous_variant | LOW | c.1365C>T|p.Phe455Phe |
S107 |
10 | BAA06g41350 | A06 | 26908802 | C | T | missense_variant | MODERATE | c.328G>A|p.Glu110Lys |
S192 |
11 | BAA06g41350 | A06 | 26908976 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S161 |
12 | BAA06g41350 | A06 | 26909349 | C | T | upstream_gene_variant | MODIFIER | c.-220G>A| |
S116 |
13 | BAA06g41350 | A06 | 26910651 | G | A | upstream_gene_variant | MODIFIER | c.-1522C>T| |
S98 |
14 | BAA06g41350 | A06 | 26911155 | C | T | upstream_gene_variant | MODIFIER | c.-2026G>A| |
S146 |
15 | BAA06g41350 | A06 | 26911460 | G | A | upstream_gene_variant | MODIFIER | c.-2331C>T| |
S284 |
16 | BAA06g41350 | A06 | 26911931 | T | C | upstream_gene_variant | MODIFIER | c.-2802A>G| |
S193 |
17 | BAA06g41350 | A06 | 26911940 | G | A | upstream_gene_variant | MODIFIER | c.-2811C>T| |
S36 |
18 | BAA06g41350 | A06 | 26912830 | G | A | upstream_gene_variant | MODIFIER | c.-3701C>T| |
S28 |
19 | BAA06g41350 | A06 | 26913730 | C | T | upstream_gene_variant | MODIFIER | c.-4601G>A| |
S30 S31 |