Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19650 | A10 | 17959425 | C | T | downstream_gene_variant | MODIFIER | c.*3579G>A| |
S70 |
2 | BAA10g19650 | A10 | 17960232 | G | A | downstream_gene_variant | MODIFIER | c.*2772C>T| |
S159 S243 |
3 | BAA10g19650 | A10 | 17960564 | C | T | downstream_gene_variant | MODIFIER | c.*2440G>A| |
S23 |
4 | BAA10g19650 | A10 | 17960921 | G | A | downstream_gene_variant | MODIFIER | c.*2083C>T| |
S4 |
5 | BAA10g19650 | A10 | 17961987 | C | T | downstream_gene_variant | MODIFIER | c.*1017G>A| |
S89 |
6 | BAA10g19650 | A10 | 17962363 | C | T | downstream_gene_variant | MODIFIER | c.*641G>A| |
S187 S243 S298 |
7 | BAA10g19650 | A10 | 17962501 | G | A | downstream_gene_variant | MODIFIER | c.*503C>T| |
S163 |
8 | BAA10g19650 | A10 | 17962753 | G | A | downstream_gene_variant | MODIFIER | c.*251C>T| |
S4 |
9 | BAA10g19650 | A10 | 17963327 | G | A | missense_variant | MODERATE | c.1411C>T|p.Pro471Ser |
S139 |
10 | BAA10g19650 | A10 | 17963530 | C | T | missense_variant | MODERATE | c.1208G>A|p.Gly403Glu |
S73 S91 |
11 | BAA10g19650 | A10 | 17963724 | C | T | synonymous_variant | LOW | c.1014G>A|p.Glu338Glu |
S148 S30 S31 |
12 | BAA10g19650 | A10 | 17965166 | G | A | synonymous_variant | LOW | c.612C>T|p.Ser204Ser |
S262 |
13 | BAA10g19650 | A10 | 17967063 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S239 |
14 | BAA10g19650 | A10 | 17967624 | G | A | upstream_gene_variant | MODIFIER | c.-732C>T| |
S219 |
15 | BAA10g19650 | A10 | 17968388 | G | A | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S1 S113 S115 S117 S122 S161 S19 S228 S244 S251 S289 S290 S297 S305 S35 S5 S65 S8 S90 |
16 | BAA10g19650 | A10 | 17970876 | C | T | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S96 |
17 | BAA10g19650 | A10 | 17971061 | C | T | upstream_gene_variant | MODIFIER | c.-4169G>A| |
S153 S213 |