Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38420 | A06 | 25164871 | C | T | missense_variant | MODERATE | c.759G>A|p.Met253Ile |
S270 |
2 | BAA06g38420 | A06 | 25172674 | G | A | intron_variant | MODIFIER | c.243+5325C>T| |
S191 |
3 | BAA06g38420 | A06 | 25173343 | G | A | intron_variant | MODIFIER | c.243+4656C>T| |
S302 |
4 | BAA06g38420 | A06 | 25173427 | C | T | intron_variant | MODIFIER | c.243+4572G>A| |
S143 |
5 | BAA06g38420 | A06 | 25174346 | G | A | intron_variant | MODIFIER | c.243+3653C>T| |
S177 |
6 | BAA06g38420 | A06 | 25174361 | T | C | intron_variant | MODIFIER | c.243+3638A>G| |
S134 |
7 | BAA06g38420 | A06 | 25174504 | C | T | intron_variant | MODIFIER | c.243+3495G>A| |
S167 |
8 | BAA06g38420 | A06 | 25175163 | C | T | intron_variant | MODIFIER | c.243+2836G>A| |
S87 |
9 | BAA06g38420 | A06 | 25175644 | G | A | intron_variant | MODIFIER | c.243+2355C>T| |
S275 |
10 | BAA06g38420 | A06 | 25175911 | G | A | intron_variant | MODIFIER | c.243+2088C>T| |
S204 |
11 | BAA06g38420 | A06 | 25177283 | C | T | intron_variant | MODIFIER | c.243+716G>A| |
S111 |
12 | BAA06g38420 | A06 | 25177365 | C | T | intron_variant | MODIFIER | c.243+634G>A| |
S46 |
13 | BAA06g38420 | A06 | 25177854 | C | T | intron_variant | MODIFIER | c.243+145G>A| |
S189 |
14 | BAA06g38420 | A06 | 25178289 | G | A | intron_variant | MODIFIER | c.73+119C>T| |
S47 |
15 | BAA06g38420 | A06 | 25179713 | C | T | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S235 |
16 | BAA06g38420 | A06 | 25180640 | C | T | upstream_gene_variant | MODIFIER | c.-2160G>A| |
S205 |
17 | BAA06g38420 | A06 | 25181140 | G | A | upstream_gene_variant | MODIFIER | c.-2660C>T| |
S117 |
18 | BAA06g38420 | A06 | 25181973 | C | T | upstream_gene_variant | MODIFIER | c.-3493G>A| |
S109 |
19 | BAA06g38420 | A06 | 25182267 | G | A | upstream_gene_variant | MODIFIER | c.-3787C>T| |
S271 |
20 | BAA06g38420 | A06 | 25183153 | G | A | upstream_gene_variant | MODIFIER | c.-4673C>T| |
S152 |