Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g32540 | A05 | 34663715 | G | A | missense_variant | MODERATE | c.2048C>T|p.Ser683Leu |
S156 |
2 | BAA05g32540 | A05 | 34664818 | G | A | missense_variant | MODERATE | c.1984C>T|p.Pro662Ser |
S150 |
3 | BAA05g32540 | A05 | 34665628 | C | T | missense_variant | MODERATE | c.1648G>A|p.Val550Ile |
S10 |
4 | BAA05g32540 | A05 | 34666151 | G | A | missense_variant | MODERATE | c.1207C>T|p.Leu403Phe |
S177 |
5 | BAA05g32540 | A05 | 34666805 | C | T | intron_variant | MODIFIER | c.984-17G>A| |
S239 |
6 | BAA05g32540 | A05 | 34667259 | C | T | missense_variant | MODERATE | c.785G>A|p.Ser262Asn |
S165 |
7 | BAA05g32540 | A05 | 34667449 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.696-1G>A| |
S130 |
8 | BAA05g32540 | A05 | 34667716 | C | T | splice_region_variant&intron_variant | LOW | c.623+5G>A| |
S42 |
9 | BAA05g32540 | A05 | 34669573 | G | A | missense_variant | MODERATE | c.191C>T|p.Thr64Ile |
S252 |
10 | BAA05g32540 | A05 | 34669613 | C | T | missense_variant | MODERATE | c.151G>A|p.Asp51Asn |
S9 |
11 | BAA05g32540 | A05 | 34671776 | C | T | upstream_gene_variant | MODIFIER | c.-1920G>A| |
S195 |
12 | BAA05g32540 | A05 | 34671967 | G | A | upstream_gene_variant | MODIFIER | c.-2111C>T| |
S250 |
13 | BAA05g32540 | A05 | 34673086 | G | A | upstream_gene_variant | MODIFIER | c.-3230C>T| |
S245 |
14 | BAA05g32540 | A05 | 34673593 | C | T | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S119 |
15 | BAA05g32540 | A05 | 34673708 | C | T | upstream_gene_variant | MODIFIER | c.-3852G>A| |
S99 |
16 | BAA05g32540 | A05 | 34674138 | G | A | upstream_gene_variant | MODIFIER | c.-4282C>T| |
S20 |