Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10620 | A04 | 16714622 | C | T | upstream_gene_variant | MODIFIER | c.-806C>T| |
S296 |
2 | BAA04g10620 | A04 | 16714830 | A | G | upstream_gene_variant | MODIFIER | c.-598A>G| |
S5 |
3 | BAA04g10620 | A04 | 16715447 | C | T | missense_variant | MODERATE | c.20C>T|p.Thr7Ile |
S204 |
4 | BAA04g10620 | A04 | 16715469 | C | T | synonymous_variant | LOW | c.42C>T|p.Leu14Leu |
S274 |
5 | BAA04g10620 | A04 | 16716324 | C | T | synonymous_variant | LOW | c.669C>T|p.Cys223Cys |
S132 S137 S215 S89 |
6 | BAA04g10620 | A04 | 16716650 | C | T | synonymous_variant | LOW | c.877C>T|p.Leu293Leu |
S179 |
7 | BAA04g10620 | A04 | 16718922 | G | A | missense_variant&splice_region_variant | MODERATE | c.2279G>A|p.Gly760Glu |
S183 S198 |
8 | BAA04g10620 | A04 | 16719012 | C | T | missense_variant | MODERATE | c.2369C>T|p.Ser790Leu |
S202 |
9 | BAA04g10620 | A04 | 16719027 | G | A | missense_variant | MODERATE | c.2384G>A|p.Arg795His |
S35 |
10 | BAA04g10620 | A04 | 16719779 | C | T | missense_variant | MODERATE | c.2903C>T|p.Ser968Phe |
S76 |
11 | BAA04g10620 | A04 | 16719809 | C | T | missense_variant | MODERATE | c.2933C>T|p.Ser978Phe |
S92 |
12 | BAA04g10620 | A04 | 16719940 | G | A | missense_variant | MODERATE | c.3064G>A|p.Val1022Ile |
S133 |
13 | BAA04g10620 | A04 | 16720555 | G | A | downstream_gene_variant | MODIFIER | c.*568G>A| |
S216 |