Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g21430 | A05 | 13699376 | G | A | missense_variant | MODERATE | c.1363C>T|p.Pro455Ser |
S187 |
2 | BAA05g21430 | A05 | 13699595 | G | C | missense_variant | MODERATE | c.1144C>G|p.Arg382Gly |
S138 S238 S288 |
3 | BAA05g21430 | A05 | 13699722 | G | A | synonymous_variant | LOW | c.1017C>T|p.Ile339Ile |
S134 |
4 | BAA05g21430 | A05 | 13699962 | G | A | missense_variant | MODERATE | c.842C>T|p.Pro281Leu |
S156 |
5 | BAA05g21430 | A05 | 13700018 | G | A | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S3 |
6 | BAA05g21430 | A05 | 13700269 | C | T | missense_variant | MODERATE | c.596G>A|p.Arg199His |
S50 |
7 | BAA05g21430 | A05 | 13700512 | C | T | missense_variant | MODERATE | c.415G>A|p.Val139Ile |
S58 |
8 | BAA05g21430 | A05 | 13701439 | C | T | upstream_gene_variant | MODIFIER | c.-449G>A| |
S241 |
9 | BAA05g21430 | A05 | 13701679 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S69 |
10 | BAA05g21430 | A05 | 13702256 | G | A | upstream_gene_variant | MODIFIER | c.-1266C>T| |
S39 |
11 | BAA05g21430 | A05 | 13702628 | G | A | upstream_gene_variant | MODIFIER | c.-1638C>T| |
S79 S91 |
12 | BAA05g21430 | A05 | 13703785 | G | A | upstream_gene_variant | MODIFIER | c.-2795C>T| |
S260 |
13 | BAA05g21430 | A05 | 13704523 | C | T | upstream_gene_variant | MODIFIER | c.-3533G>A| |
S121 |