Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g24460 | A05 | 29372469 | G | A | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S301 S304 |
2 | BAA05g24460 | A05 | 29372687 | C | T | upstream_gene_variant | MODIFIER | c.-3804C>T| |
S47 |
3 | BAA05g24460 | A05 | 29377161 | G | A | missense_variant | MODERATE | c.671G>A|p.Gly224Glu |
S76 |
4 | BAA05g24460 | A05 | 29377417 | C | T | synonymous_variant | LOW | c.927C>T|p.Asn309Asn |
S273 |
5 | BAA05g24460 | A05 | 29377451 | G | A | missense_variant | MODERATE | c.961G>A|p.Asp321Asn |
S203 |
6 | BAA05g24460 | A05 | 29377515 | C | T | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S103 |
7 | BAA05g24460 | A05 | 29377985 | G | A | missense_variant | MODERATE | c.1495G>A|p.Val499Met |
S189 S243 S299 |
8 | BAA05g24460 | A05 | 29378169 | G | A | missense_variant | MODERATE | c.1679G>A|p.Arg560Lys |
S109 |
9 | BAA05g24460 | A05 | 29378661 | G | A | missense_variant | MODERATE | c.2171G>A|p.Arg724His |
S82 S92 |
10 | BAA05g24460 | A05 | 29378918 | G | A | missense_variant | MODERATE | c.2428G>A|p.Ala810Thr |
S134 |
11 | BAA05g24460 | A05 | 29379418 | C | T | synonymous_variant | LOW | c.2928C>T|p.Pro976Pro |
S175 S177 |
12 | BAA05g24460 | A05 | 29381035 | C | T | downstream_gene_variant | MODIFIER | c.*1506C>T| |
S251 |
13 | BAA05g24460 | A05 | 29382621 | G | A | downstream_gene_variant | MODIFIER | c.*3092G>A| |
S163 |
14 | BAA05g24460 | A05 | 29382966 | C | T | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S8 |
15 | BAA05g24460 | A05 | 29384045 | C | T | downstream_gene_variant | MODIFIER | c.*4516C>T| |
S19 |
16 | BAA05g24460 | A05 | 29384357 | C | T | downstream_gene_variant | MODIFIER | c.*4828C>T| |
S19 |
17 | BAA05g24460 | A05 | 29384385 | G | A | downstream_gene_variant | MODIFIER | c.*4856G>A| |
S123 |