Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31510 | A02 | 18945096 | C | T | missense_variant | MODERATE | c.3109G>A|p.Glu1037Lys |
S8 |
2 | BAA02g31510 | A02 | 18945818 | G | A | splice_region_variant&intron_variant | LOW | c.2969+6C>T| |
S45 |
3 | BAA02g31510 | A02 | 18946038 | G | A | missense_variant | MODERATE | c.2755C>T|p.Pro919Ser |
S47 |
4 | BAA02g31510 | A02 | 18946224 | G | A | missense_variant | MODERATE | c.2569C>T|p.Leu857Phe |
S134 |
5 | BAA02g31510 | A02 | 18946788 | G | A | missense_variant | MODERATE | c.2159C>T|p.Pro720Leu |
S302 |
6 | BAA02g31510 | A02 | 18946977 | G | A | missense_variant | MODERATE | c.2062C>T|p.Pro688Ser |
S174 |
7 | BAA02g31510 | A02 | 18947535 | C | T | missense_variant | MODERATE | c.1504G>A|p.Val502Ile |
S131 |
8 | BAA02g31510 | A02 | 18947667 | C | T | splice_region_variant&intron_variant | LOW | c.1405-4G>A| |
S182 |
9 | BAA02g31510 | A02 | 18947821 | G | A | missense_variant | MODERATE | c.1333C>T|p.Pro445Ser |
S71 |
10 | BAA02g31510 | A02 | 18948144 | G | A | synonymous_variant | LOW | c.1266C>T|p.Arg422Arg |
S48 |
11 | BAA02g31510 | A02 | 18948160 | G | A | missense_variant | MODERATE | c.1250C>T|p.Ser417Leu |
S191 |
12 | BAA02g31510 | A02 | 18948360 | G | A | synonymous_variant | LOW | c.1050C>T|p.Asp350Asp |
S249 |
13 | BAA02g31510 | A02 | 18948733 | G | A | missense_variant | MODERATE | c.761C>T|p.Ser254Phe |
S166 |
14 | BAA02g31510 | A02 | 18949127 | C | T | missense_variant | MODERATE | c.367G>A|p.Gly123Ser |
S88 |
15 | BAA02g31510 | A02 | 18949603 | C | T | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S242 |
16 | BAA02g31510 | A02 | 18949720 | C | T | upstream_gene_variant | MODIFIER | c.-69G>A| |
S301 |
17 | BAA02g31510 | A02 | 18952848 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S201 |