Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05710 | A10 | 2922145 | G | A | synonymous_variant | LOW | c.3003C>T|p.Phe1001Phe |
S105 S106 |
2 | BAA10g05710 | A10 | 2922664 | C | T | synonymous_variant | LOW | c.2568G>A|p.Lys856Lys |
S119 |
3 | BAA10g05710 | A10 | 2922825 | C | T | missense_variant | MODERATE | c.2407G>A|p.Glu803Lys |
S260 |
4 | BAA10g05710 | A10 | 2923082 | G | A | missense_variant | MODERATE | c.2150C>T|p.Thr717Ile |
S198 |
5 | BAA10g05710 | A10 | 2924683 | A | G | synonymous_variant | LOW | c.1245T>C|p.Tyr415Tyr |
S159 S243 S81 |
6 | BAA10g05710 | A10 | 2924831 | G | A | missense_variant | MODERATE | c.1166C>T|p.Ala389Val |
S157 S163 |
7 | BAA10g05710 | A10 | 2925713 | G | A | splice_region_variant&intron_variant | LOW | c.840+6C>T| |
S136 |
8 | BAA10g05710 | A10 | 2927391 | C | T | upstream_gene_variant | MODIFIER | c.-491G>A| |
S70 |
9 | BAA10g05710 | A10 | 2927394 | G | A | upstream_gene_variant | MODIFIER | c.-494C>T| |
S242 |
10 | BAA10g05710 | A10 | 2929781 | G | A | upstream_gene_variant | MODIFIER | c.-2881C>T| |
S100 |