Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10380 | A10 | 12120358 | C | T | upstream_gene_variant | MODIFIER | c.-2926C>T| |
S146 |
2 | BAA10g10380 | A10 | 12121272 | G | A | upstream_gene_variant | MODIFIER | c.-2012G>A| |
S251 |
3 | BAA10g10380 | A10 | 12121360 | G | A | upstream_gene_variant | MODIFIER | c.-1924G>A| |
S305 |
4 | BAA10g10380 | A10 | 12121756 | G | A | upstream_gene_variant | MODIFIER | c.-1528G>A| |
S148 S30 S31 |
5 | BAA10g10380 | A10 | 12122157 | C | T | upstream_gene_variant | MODIFIER | c.-1127C>T| |
S92 |
6 | BAA10g10380 | A10 | 12122437 | C | T | upstream_gene_variant | MODIFIER | c.-847C>T| |
S76 |
7 | BAA10g10380 | A10 | 12122567 | C | T | upstream_gene_variant | MODIFIER | c.-717C>T| |
S42 |
8 | BAA10g10380 | A10 | 12123249 | C | T | upstream_gene_variant | MODIFIER | c.-35C>T| |
S136 S186 |
9 | BAA10g10380 | A10 | 12123414 | C | T | missense_variant | MODERATE | c.131C>T|p.Ser44Phe |
S97 |
10 | BAA10g10380 | A10 | 12123573 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S243 S298 S299 |
11 | BAA10g10380 | A10 | 12124103 | G | A | missense_variant | MODERATE | c.820G>A|p.Ala274Thr |
S284 |
12 | BAA10g10380 | A10 | 12124348 | C | T | synonymous_variant | LOW | c.1065C>T|p.Leu355Leu |
S301 S304 |
13 | BAA10g10380 | A10 | 12124383 | C | T | missense_variant | MODERATE | c.1100C>T|p.Thr367Ile |
S165 S211 S227 |