Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12640 | A10 | 14025771 | C | T | upstream_gene_variant | MODIFIER | c.-4922C>T| |
S68 |
2 | BAA10g12640 | A10 | 14025773 | C | T | upstream_gene_variant | MODIFIER | c.-4920C>T| |
S247 |
3 | BAA10g12640 | A10 | 14026458 | C | T | upstream_gene_variant | MODIFIER | c.-4235C>T| |
S42 |
4 | BAA10g12640 | A10 | 14027749 | C | T | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S144 |
5 | BAA10g12640 | A10 | 14028816 | C | T | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S56 |
6 | BAA10g12640 | A10 | 14030219 | C | T | upstream_gene_variant | MODIFIER | c.-474C>T| |
S27 |
7 | BAA10g12640 | A10 | 14030828 | G | A | splice_region_variant&intron_variant | LOW | c.31-4G>A| |
S288 |
8 | BAA10g12640 | A10 | 14031321 | C | T | downstream_gene_variant | MODIFIER | c.*120C>T| |
S20 |
9 | BAA10g12640 | A10 | 14031432 | C | T | downstream_gene_variant | MODIFIER | c.*231C>T| |
S166 |
10 | BAA10g12640 | A10 | 14033250 | C | T | downstream_gene_variant | MODIFIER | c.*2049C>T| |
S131 |
11 | BAA10g12640 | A10 | 14033293 | C | T | downstream_gene_variant | MODIFIER | c.*2092C>T| |
S84 S93 |
12 | BAA10g12640 | A10 | 14033397 | G | A | downstream_gene_variant | MODIFIER | c.*2196G>A| |
S159 S243 |
13 | BAA10g12640 | A10 | 14034658 | C | T | downstream_gene_variant | MODIFIER | c.*3457C>T| |
S5 |
14 | BAA10g12640 | A10 | 14035613 | C | T | downstream_gene_variant | MODIFIER | c.*4412C>T| |
S176 |
15 | BAA10g12640 | A10 | 14035662 | G | A | downstream_gene_variant | MODIFIER | c.*4461G>A| |
S125 |
16 | BAA10g12640 | A10 | 14035879 | G | A | downstream_gene_variant | MODIFIER | c.*4678G>A| |
S71 |
17 | BAA10g12640 | A10 | 14036108 | G | A | downstream_gene_variant | MODIFIER | c.*4907G>A| |
S9 |