Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g03170 | A05 | 1625754 | C | T | downstream_gene_variant | MODIFIER | c.*2079G>A| |
S203 |
2 | BAA05g03170 | A05 | 1628234 | C | T | missense_variant | MODERATE | c.2561G>A|p.Arg854Gln |
S303 S304 |
3 | BAA05g03170 | A05 | 1628439 | C | T | missense_variant | MODERATE | c.2356G>A|p.Gly786Ser |
S270 |
4 | BAA05g03170 | A05 | 1629026 | C | T | missense_variant | MODERATE | c.2182G>A|p.Glu728Lys |
S262 |
5 | BAA05g03170 | A05 | 1629334 | C | T | missense_variant | MODERATE | c.1874G>A|p.Gly625Glu |
S128 |
6 | BAA05g03170 | A05 | 1630314 | C | T | synonymous_variant | LOW | c.1206G>A|p.Val402Val |
S208 S93 |
7 | BAA05g03170 | A05 | 1630580 | G | A | synonymous_variant | LOW | c.1011C>T|p.Arg337Arg |
S242 |
8 | BAA05g03170 | A05 | 1631789 | C | T | missense_variant | MODERATE | c.472G>A|p.Asp158Asn |
S36 |
9 | BAA05g03170 | A05 | 1631888 | C | T | missense_variant | MODERATE | c.373G>A|p.Gly125Arg |
S236 |
10 | BAA05g03170 | A05 | 1631942 | G | A | missense_variant | MODERATE | c.319C>T|p.Leu107Phe |
S178 |
11 | BAA05g03170 | A05 | 1632112 | C | T | intron_variant | MODIFIER | c.169-20G>A| |
S256 |
12 | BAA05g03170 | A05 | 1632347 | C | T | synonymous_variant | LOW | c.24G>A|p.Lys8Lys |
S239 |
13 | BAA05g03170 | A05 | 1633170 | G | A | upstream_gene_variant | MODIFIER | c.-800C>T| |
S178 |
14 | BAA05g03170 | A05 | 1634570 | G | A | upstream_gene_variant | MODIFIER | c.-2200C>T| |
S200 |
15 | BAA05g03170 | A05 | 1635879 | G | A | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S150 |
16 | BAA05g03170 | A05 | 1635885 | G | A | upstream_gene_variant | MODIFIER | c.-3515C>T| |
S264 |
17 | BAA05g03170 | A05 | 1636093 | G | A | upstream_gene_variant | MODIFIER | c.-3723C>T| |
S124 |