Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g21400 | A07 | 26138175 | G | A | upstream_gene_variant | MODIFIER | c.-800G>A| |
S28 |
2 | BAA07g21400 | A07 | 26138568 | G | A | upstream_gene_variant | MODIFIER | c.-407G>A| |
S208 |
3 | BAA07g21400 | A07 | 26139745 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.349-1G>A| |
S296 |
4 | BAA07g21400 | A07 | 26140171 | G | A | missense_variant | MODERATE | c.610G>A|p.Ala204Thr |
S185 |
5 | BAA07g21400 | A07 | 26140637 | C | T | missense_variant | MODERATE | c.860C>T|p.Ser287Phe |
S245 |
6 | BAA07g21400 | A07 | 26140977 | C | T | synonymous_variant | LOW | c.1101C>T|p.Gly367Gly |
S123 |
7 | BAA07g21400 | A07 | 26141362 | C | T | synonymous_variant | LOW | c.1422C>T|p.Gly474Gly |
S162 |
8 | BAA07g21400 | A07 | 26143943 | G | A | downstream_gene_variant | MODIFIER | c.*1453G>A| |
S276 |
9 | BAA07g21400 | A07 | 26144363 | C | T | downstream_gene_variant | MODIFIER | c.*1873C>T| |
S32 |
10 | BAA07g21400 | A07 | 26144619 | G | A | downstream_gene_variant | MODIFIER | c.*2129G>A| |
S107 |
11 | BAA07g21400 | A07 | 26144676 | C | T | downstream_gene_variant | MODIFIER | c.*2186C>T| |
S42 |
12 | BAA07g21400 | A07 | 26144707 | C | T | downstream_gene_variant | MODIFIER | c.*2217C>T| |
S249 |
13 | BAA07g21400 | A07 | 26145034 | G | A | downstream_gene_variant | MODIFIER | c.*2544G>A| |
S135 |
14 | BAA07g21400 | A07 | 26146600 | C | T | downstream_gene_variant | MODIFIER | c.*4110C>T| |
S181 |
15 | BAA07g21400 | A07 | 26147251 | C | T | downstream_gene_variant | MODIFIER | c.*4761C>T| |
S96 |