Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11170 | A07 | 19924106 | C | T | upstream_gene_variant | MODIFIER | c.-4976C>T| |
S242 |
2 | BAA07g11170 | A07 | 19924124 | C | T | upstream_gene_variant | MODIFIER | c.-4958C>T| |
S38 |
3 | BAA07g11170 | A07 | 19924264 | C | T | upstream_gene_variant | MODIFIER | c.-4818C>T| |
S114 |
4 | BAA07g11170 | A07 | 19924379 | C | T | upstream_gene_variant | MODIFIER | c.-4703C>T| |
S166 |
5 | BAA07g11170 | A07 | 19925052 | C | T | upstream_gene_variant | MODIFIER | c.-4030C>T| |
S276 |
6 | BAA07g11170 | A07 | 19925927 | C | T | upstream_gene_variant | MODIFIER | c.-3155C>T| |
S301 S304 |
7 | BAA07g11170 | A07 | 19929216 | G | A | synonymous_variant | LOW | c.135G>A|p.Glu45Glu |
S48 |
8 | BAA07g11170 | A07 | 19929405 | G | A | intron_variant | MODIFIER | c.193+131G>A| |
S210 S225 |
9 | BAA07g11170 | A07 | 19930010 | G | A | missense_variant | MODERATE | c.353G>A|p.Gly118Asp |
S82 S92 |
10 | BAA07g11170 | A07 | 19930525 | C | T | missense_variant | MODERATE | c.785C>T|p.Ala262Val |
S18 |