Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19200 | A05 | 11243976 | C | T | intron_variant | MODIFIER | c.1661-851G>A| |
S185 |
2 | BAA05g19200 | A05 | 11244791 | G | A | intron_variant | MODIFIER | c.1660+1437C>T| |
S172 S217 |
3 | BAA05g19200 | A05 | 11245059 | G | A | intron_variant | MODIFIER | c.1660+1169C>T| |
S278 |
4 | BAA05g19200 | A05 | 11245103 | G | A | intron_variant | MODIFIER | c.1660+1125C>T| |
S192 |
5 | BAA05g19200 | A05 | 11245325 | G | A | intron_variant | MODIFIER | c.1660+903C>T| |
S217 S248 |
6 | BAA05g19200 | A05 | 11247286 | A | G | missense_variant | MODERATE | c.911T>C|p.Ile304Thr |
S151 S263 |
7 | BAA05g19200 | A05 | 11248616 | C | T | missense_variant | MODERATE | c.164G>A|p.Gly55Asp |
S153 S213 |
8 | BAA05g19200 | A05 | 11249355 | G | A | upstream_gene_variant | MODIFIER | c.-345C>T| |
S212 S259 |
9 | BAA05g19200 | A05 | 11249453 | C | T | upstream_gene_variant | MODIFIER | c.-443G>A| |
S113 |
10 | BAA05g19200 | A05 | 11249601 | C | T | upstream_gene_variant | MODIFIER | c.-591G>A| |
S43 |
11 | BAA05g19200 | A05 | 11250858 | C | T | upstream_gene_variant | MODIFIER | c.-1848G>A| |
S18 |
12 | BAA05g19200 | A05 | 11251199 | C | T | upstream_gene_variant | MODIFIER | c.-2189G>A| |
S280 |
13 | BAA05g19200 | A05 | 11252117 | T | A | upstream_gene_variant | MODIFIER | c.-3107A>T| |
S301 S304 |
14 | BAA05g19200 | A05 | 11252653 | G | A | upstream_gene_variant | MODIFIER | c.-3643C>T| |
S79 S84 |
15 | BAA05g19200 | A05 | 11252659 | G | A | upstream_gene_variant | MODIFIER | c.-3649C>T| |
S38 |
16 | BAA05g19200 | A05 | 11253713 | C | T | upstream_gene_variant | MODIFIER | c.-4703G>A| |
S240 |