Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11590 | A10 | 13189842 | C | T | upstream_gene_variant | MODIFIER | c.-3733C>T| |
S42 |
2 | BAA10g11590 | A10 | 13190913 | C | T | upstream_gene_variant | MODIFIER | c.-2662C>T| |
S274 |
3 | BAA10g11590 | A10 | 13193450 | G | A | upstream_gene_variant | MODIFIER | c.-125G>A| |
S1 S90 |
4 | BAA10g11590 | A10 | 13193656 | G | A | missense_variant | MODERATE | c.82G>A|p.Glu28Lys |
S65 |
5 | BAA10g11590 | A10 | 13194547 | C | T | missense_variant | MODERATE | c.496C>T|p.Leu166Phe |
S79 S91 |
6 | BAA10g11590 | A10 | 13195008 | C | T | synonymous_variant | LOW | c.873C>T|p.Val291Val |
S6 |
7 | BAA10g11590 | A10 | 13195225 | G | A | missense_variant | MODERATE | c.1090G>A|p.Ala364Thr |
S295 |
8 | BAA10g11590 | A10 | 13195259 | C | T | missense_variant | MODERATE | c.1124C>T|p.Ser375Phe |
S143 |
9 | BAA10g11590 | A10 | 13196359 | G | A | missense_variant | MODERATE | c.1772G>A|p.Gly591Glu |
S221 |
10 | BAA10g11590 | A10 | 13196588 | C | T | synonymous_variant | LOW | c.2001C>T|p.His667His |
S282 |
11 | BAA10g11590 | A10 | 13197166 | C | T | downstream_gene_variant | MODIFIER | c.*353C>T| |
S238 |
12 | BAA10g11590 | A10 | 13197176 | C | T | downstream_gene_variant | MODIFIER | c.*363C>T| |
S247 |
13 | BAA10g11590 | A10 | 13197348 | C | T | downstream_gene_variant | MODIFIER | c.*535C>T| |
S277 |
14 | BAA10g11590 | A10 | 13197615 | C | T | downstream_gene_variant | MODIFIER | c.*802C>T| |
S23 |
15 | BAA10g11590 | A10 | 13197718 | T | C | downstream_gene_variant | MODIFIER | c.*905T>C| |
S66 |
16 | BAA10g11590 | A10 | 13197756 | G | A | downstream_gene_variant | MODIFIER | c.*943G>A| |
S149 S303 |
17 | BAA10g11590 | A10 | 13198582 | C | T | downstream_gene_variant | MODIFIER | c.*1769C>T| |
S23 |
18 | BAA10g11590 | A10 | 13199608 | C | T | downstream_gene_variant | MODIFIER | c.*2795C>T| |
S195 |
19 | BAA10g11590 | A10 | 13199854 | C | T | downstream_gene_variant | MODIFIER | c.*3041C>T| |
S193 |