Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g30580 | A05 | 33569708 | G | A | synonymous_variant | LOW | c.2505C>T|p.Leu835Leu |
S228 |
2 | BAA05g30580 | A05 | 33570132 | G | A | stop_gained | HIGH | c.2173C>T|p.Gln725* |
S44 |
3 | BAA05g30580 | A05 | 33570205 | C | T | synonymous_variant | LOW | c.2100G>A|p.Lys700Lys |
S25 |
4 | BAA05g30580 | A05 | 33570280 | C | T | synonymous_variant | LOW | c.2025G>A|p.Leu675Leu |
S67 |
5 | BAA05g30580 | A05 | 33570623 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1683-1G>A| |
S273 |
6 | BAA05g30580 | A05 | 33571144 | C | T | missense_variant | MODERATE | c.1627G>A|p.Asp543Asn |
S36 |
7 | BAA05g30580 | A05 | 33571230 | G | A | missense_variant | MODERATE | c.1541C>T|p.Ser514Phe |
S50 |
8 | BAA05g30580 | A05 | 33571944 | G | A | missense_variant | MODERATE | c.977C>T|p.Thr326Ile |
S212 |
9 | BAA05g30580 | A05 | 33573113 | C | T | intron_variant | MODIFIER | c.310-20G>A| |
S171 |
10 | BAA05g30580 | A05 | 33573762 | G | A | intron_variant | MODIFIER | c.67+29C>T| |
S256 |
11 | BAA05g30580 | A05 | 33574550 | C | T | upstream_gene_variant | MODIFIER | c.-693G>A| |
S17 |
12 | BAA05g30580 | A05 | 33575110 | A | T | upstream_gene_variant | MODIFIER | c.-1253T>A| |
S179 |
13 | BAA05g30580 | A05 | 33575894 | G | A | upstream_gene_variant | MODIFIER | c.-2037C>T| |
S240 |
14 | BAA05g30580 | A05 | 33576432 | G | A | upstream_gene_variant | MODIFIER | c.-2575C>T| |
S80 |
15 | BAA05g30580 | A05 | 33578092 | C | T | upstream_gene_variant | MODIFIER | c.-4235G>A| |
S128 |
16 | BAA05g30580 | A05 | 33578117 | G | A | upstream_gene_variant | MODIFIER | c.-4260C>T| |
S69 |