Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41650 | A09 | 48322306 | G | A | missense_variant | MODERATE | c.1933C>T|p.Pro645Ser |
S12 |
2 | BAA09g41650 | A09 | 48322391 | C | T | synonymous_variant | LOW | c.1848G>A|p.Glu616Glu |
S234 |
3 | BAA09g41650 | A09 | 48322801 | C | T | missense_variant | MODERATE | c.1646G>A|p.Arg549His |
S186 |
4 | BAA09g41650 | A09 | 48323294 | G | A | synonymous_variant | LOW | c.1434C>T|p.Val478Val |
S202 |
5 | BAA09g41650 | A09 | 48324343 | C | T | missense_variant | MODERATE | c.1082G>A|p.Arg361Gln |
S117 |
6 | BAA09g41650 | A09 | 48325005 | C | T | missense_variant | MODERATE | c.799G>A|p.Ala267Thr |
S136 |
7 | BAA09g41650 | A09 | 48325471 | C | T | splice_region_variant&intron_variant | LOW | c.493-4G>A| |
S94 |
8 | BAA09g41650 | A09 | 48325654 | C | T | missense_variant | MODERATE | c.382G>A|p.Glu128Lys |
S32 |
9 | BAA09g41650 | A09 | 48325699 | G | A | missense_variant | MODERATE | c.337C>T|p.Arg113Trp |
S188 |
10 | BAA09g41650 | A09 | 48325766 | C | T | synonymous_variant | LOW | c.270G>A|p.Ala90Ala |
S282 |
11 | BAA09g41650 | A09 | 48327127 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S10 |
12 | BAA09g41650 | A09 | 48327372 | G | A | upstream_gene_variant | MODIFIER | c.-1337C>T| |
S196 |
13 | BAA09g41650 | A09 | 48327388 | C | T | upstream_gene_variant | MODIFIER | c.-1353G>A| |
S50 |
14 | BAA09g41650 | A09 | 48329205 | C | T | upstream_gene_variant | MODIFIER | c.-3170G>A| |
S19 |