Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10160 | A10 | 11929100 | G | A | downstream_gene_variant | MODIFIER | c.*4024C>T| |
S226 |
2 | BAA10g10160 | A10 | 11929303 | C | T | downstream_gene_variant | MODIFIER | c.*3821G>A| |
S287 |
3 | BAA10g10160 | A10 | 11930202 | G | A | downstream_gene_variant | MODIFIER | c.*2922C>T| |
S134 |
4 | BAA10g10160 | A10 | 11930214 | C | T | downstream_gene_variant | MODIFIER | c.*2910G>A| |
S247 |
5 | BAA10g10160 | A10 | 11930304 | C | T | downstream_gene_variant | MODIFIER | c.*2820G>A| |
S183 |
6 | BAA10g10160 | A10 | 11930387 | C | T | downstream_gene_variant | MODIFIER | c.*2737G>A| |
S308 |
7 | BAA10g10160 | A10 | 11930527 | C | T | downstream_gene_variant | MODIFIER | c.*2597G>A| |
S185 |
8 | BAA10g10160 | A10 | 11931429 | G | A | downstream_gene_variant | MODIFIER | c.*1695C>T| |
S125 |
9 | BAA10g10160 | A10 | 11931712 | G | A | downstream_gene_variant | MODIFIER | c.*1412C>T| |
S128 |
10 | BAA10g10160 | A10 | 11933517 | G | A | missense_variant | MODERATE | c.826C>T|p.Leu276Phe |
S20 |
11 | BAA10g10160 | A10 | 11933875 | G | A | intron_variant | MODIFIER | c.552-84C>T| |
S226 |
12 | BAA10g10160 | A10 | 11934360 | C | T | synonymous_variant | LOW | c.162G>A|p.Glu54Glu |
S249 |
13 | BAA10g10160 | A10 | 11936579 | G | A | upstream_gene_variant | MODIFIER | c.-2058C>T| |
S100 |
14 | BAA10g10160 | A10 | 11936656 | G | A | upstream_gene_variant | MODIFIER | c.-2135C>T| |
S262 |
15 | BAA10g10160 | A10 | 11937491 | C | T | upstream_gene_variant | MODIFIER | c.-2970G>A| |
S110 |
16 | BAA10g10160 | A10 | 11937586 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
S150 |
17 | BAA10g10160 | A10 | 11937729 | G | A | upstream_gene_variant | MODIFIER | c.-3208C>T| |
S149 S88 |
18 | BAA10g10160 | A10 | 11937815 | G | A | upstream_gene_variant | MODIFIER | c.-3294C>T| |
S217 S224 |