Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g23080 | A07 | 27101816 | C | T | synonymous_variant | LOW | c.1542G>A|p.Pro514Pro |
S206 |
2 | BAA07g23080 | A07 | 27102151 | C | T | splice_donor_variant&intron_variant | HIGH | c.1397+1G>A| |
S190 |
3 | BAA07g23080 | A07 | 27102155 | C | T | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S213 |
4 | BAA07g23080 | A07 | 27102505 | G | A | synonymous_variant | LOW | c.1245C>T|p.Ile415Ile |
S125 |
5 | BAA07g23080 | A07 | 27103361 | G | A | missense_variant | MODERATE | c.712C>T|p.His238Tyr |
S87 |
6 | BAA07g23080 | A07 | 27103553 | C | T | missense_variant | MODERATE | c.520G>A|p.Gly174Arg |
S265 |
7 | BAA07g23080 | A07 | 27103601 | G | A | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S12 |
8 | BAA07g23080 | A07 | 27104187 | G | A | missense_variant | MODERATE | c.98C>T|p.Ala33Val |
S95 |
9 | BAA07g23080 | A07 | 27104239 | C | T | missense_variant | MODERATE | c.46G>A|p.Val16Met |
S176 |
10 | BAA07g23080 | A07 | 27104296 | C | T | upstream_gene_variant | MODIFIER | c.-12G>A| |
S162 |
11 | BAA07g23080 | A07 | 27104463 | C | T | upstream_gene_variant | MODIFIER | c.-179G>A| |
S281 |
12 | BAA07g23080 | A07 | 27105006 | G | A | upstream_gene_variant | MODIFIER | c.-722C>T| |
S2 |
13 | BAA07g23080 | A07 | 27105047 | G | A | upstream_gene_variant | MODIFIER | c.-763C>T| |
S188 |
14 | BAA07g23080 | A07 | 27106019 | C | T | upstream_gene_variant | MODIFIER | c.-1735G>A| |
S168 S32 |
15 | BAA07g23080 | A07 | 27108210 | C | T | upstream_gene_variant | MODIFIER | c.-3926G>A| |
S42 |
16 | BAA07g23080 | A07 | 27108273 | C | T | upstream_gene_variant | MODIFIER | c.-3989G>A| |
S262 |
17 | BAA07g23080 | A07 | 27108675 | C | T | upstream_gene_variant | MODIFIER | c.-4391G>A| |
S204 |
18 | BAA07g23080 | A07 | 27109173 | G | A | upstream_gene_variant | MODIFIER | c.-4889C>T| |
S189 |