Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11440 | A09 | 6415531 | G | A | missense_variant | MODERATE | c.1469C>T|p.Ala490Val |
S25 |
2 | BAA09g11440 | A09 | 6415592 | G | A | synonymous_variant | LOW | c.1408C>T|p.Leu470Leu |
S169 |
3 | BAA09g11440 | A09 | 6415599 | G | A | synonymous_variant | LOW | c.1401C>T|p.Ser467Ser |
S12 |
4 | BAA09g11440 | A09 | 6415657 | G | A | missense_variant | MODERATE | c.1343C>T|p.Ser448Phe |
S244 |
5 | BAA09g11440 | A09 | 6416034 | G | A | synonymous_variant | LOW | c.966C>T|p.Gly322Gly |
S274 |
6 | BAA09g11440 | A09 | 6416228 | G | A | missense_variant | MODERATE | c.772C>T|p.Pro258Ser |
S185 |
7 | BAA09g11440 | A09 | 6416901 | G | A | missense_variant | MODERATE | c.364C>T|p.Leu122Phe |
S151 |
8 | BAA09g11440 | A09 | 6416933 | G | A | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S46 |
9 | BAA09g11440 | A09 | 6417378 | G | A | upstream_gene_variant | MODIFIER | c.-26C>T| |
S73 |
10 | BAA09g11440 | A09 | 6417768 | C | T | upstream_gene_variant | MODIFIER | c.-416G>A| |
S37 S68 |
11 | BAA09g11440 | A09 | 6417858 | T | A | upstream_gene_variant | MODIFIER | c.-506A>T| |
S188 |
12 | BAA09g11440 | A09 | 6417924 | C | T | upstream_gene_variant | MODIFIER | c.-572G>A| |
S94 |
13 | BAA09g11440 | A09 | 6418437 | G | A | upstream_gene_variant | MODIFIER | c.-1085C>T| |
S240 |
14 | BAA09g11440 | A09 | 6418521 | G | A | upstream_gene_variant | MODIFIER | c.-1169C>T| |
S166 |
15 | BAA09g11440 | A09 | 6420709 | G | A | upstream_gene_variant | MODIFIER | c.-3357C>T| |
S6 |
16 | BAA09g11440 | A09 | 6421075 | G | A | upstream_gene_variant | MODIFIER | c.-3723C>T| |
S181 |
17 | BAA09g11440 | A09 | 6422175 | C | T | upstream_gene_variant | MODIFIER | c.-4823G>A| |
S161 |