Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14620 | A10 | 15258988 | C | T | missense_variant | MODERATE | c.2924G>A|p.Cys975Tyr |
S163 |
2 | BAA10g14620 | A10 | 15260031 | C | T | synonymous_variant | LOW | c.1881G>A|p.Arg627Arg |
S247 |
3 | BAA10g14620 | A10 | 15260681 | C | T | splice_region_variant&intron_variant | LOW | c.1300+5G>A| |
S225 S73 |
4 | BAA10g14620 | A10 | 15261346 | G | A | missense_variant | MODERATE | c.839C>T|p.Pro280Leu |
S240 |
5 | BAA10g14620 | A10 | 15262477 | G | A | synonymous_variant | LOW | c.321C>T|p.Ala107Ala |
S69 |
6 | BAA10g14620 | A10 | 15262649 | G | A | missense_variant | MODERATE | c.149C>T|p.Ala50Val |
S18 |
7 | BAA10g14620 | A10 | 15263383 | G | A | upstream_gene_variant | MODIFIER | c.-174C>T| |
S15 |
8 | BAA10g14620 | A10 | 15264073 | G | A | upstream_gene_variant | MODIFIER | c.-864C>T| |
S226 |
9 | BAA10g14620 | A10 | 15265314 | C | T | upstream_gene_variant | MODIFIER | c.-2105G>A| |
S10 |
10 | BAA10g14620 | A10 | 15267042 | G | A | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S239 |
11 | BAA10g14620 | A10 | 15267210 | G | A | upstream_gene_variant | MODIFIER | c.-4001C>T| |
S245 |