Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g25140 | A01 | 13487434 | G | A | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S297 |
2 | BAA01g25140 | A01 | 13487541 | C | T | upstream_gene_variant | MODIFIER | c.-4825C>T| |
S140 |
3 | BAA01g25140 | A01 | 13488757 | G | A | upstream_gene_variant | MODIFIER | c.-3609G>A| |
S12 |
4 | BAA01g25140 | A01 | 13488927 | G | A | upstream_gene_variant | MODIFIER | c.-3439G>A| |
S84 |
5 | BAA01g25140 | A01 | 13488931 | C | T | upstream_gene_variant | MODIFIER | c.-3435C>T| |
S198 |
6 | BAA01g25140 | A01 | 13489385 | G | A | upstream_gene_variant | MODIFIER | c.-2981G>A| |
S241 |
7 | BAA01g25140 | A01 | 13492374 | G | A | synonymous_variant | LOW | c.9G>A|p.Arg3Arg |
S236 |
8 | BAA01g25140 | A01 | 13492687 | G | A | missense_variant | MODERATE | c.322G>A|p.Asp108Asn |
S197 |
9 | BAA01g25140 | A01 | 13492798 | C | T | stop_gained | HIGH | c.433C>T|p.Gln145* |
S171 |
10 | BAA01g25140 | A01 | 13492996 | G | A | missense_variant | MODERATE | c.631G>A|p.Gly211Arg |
S207 S234 |
11 | BAA01g25140 | A01 | 13493021 | C | T | missense_variant | MODERATE | c.656C>T|p.Pro219Leu |
S148 S210 |
12 | BAA01g25140 | A01 | 13497340 | C | T | downstream_gene_variant | MODIFIER | c.*4135C>T| |
S107 |
13 | BAA01g25140 | A01 | 13497922 | G | A | downstream_gene_variant | MODIFIER | c.*4717G>A| |
S7 |
14 | BAA01g25140 | A01 | 13497954 | G | A | downstream_gene_variant | MODIFIER | c.*4749G>A| |
S191 |
15 | BAA01g25140 | A01 | 13498101 | C | T | downstream_gene_variant | MODIFIER | c.*4896C>T| |
S47 |