Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g21770 | A03 | 9836699 | C | T | downstream_gene_variant | MODIFIER | c.*4643G>A| |
S70 |
2 | BAA03g21770 | A03 | 9836927 | G | A | downstream_gene_variant | MODIFIER | c.*4415C>T| |
S149 |
3 | BAA03g21770 | A03 | 9837708 | C | T | downstream_gene_variant | MODIFIER | c.*3634G>A| |
S127 |
4 | BAA03g21770 | A03 | 9838097 | G | A | downstream_gene_variant | MODIFIER | c.*3245C>T| |
S169 |
5 | BAA03g21770 | A03 | 9839067 | A | C | downstream_gene_variant | MODIFIER | c.*2275T>G| |
S5 |
6 | BAA03g21770 | A03 | 9840089 | C | T | downstream_gene_variant | MODIFIER | c.*1253G>A| |
S279 |
7 | BAA03g21770 | A03 | 9840200 | G | A | downstream_gene_variant | MODIFIER | c.*1142C>T| |
S176 |
8 | BAA03g21770 | A03 | 9841428 | C | T | missense_variant | MODERATE | c.2209G>A|p.Val737Met |
S283 |
9 | BAA03g21770 | A03 | 9842392 | C | T | synonymous_variant | LOW | c.1245G>A|p.Gln415Gln |
S62 |
10 | BAA03g21770 | A03 | 9842416 | G | A | synonymous_variant | LOW | c.1221C>T|p.Ala407Ala |
S178 |
11 | BAA03g21770 | A03 | 9842696 | G | A | missense_variant | MODERATE | c.941C>T|p.Pro314Leu |
S128 |
12 | BAA03g21770 | A03 | 9842935 | C | T | synonymous_variant | LOW | c.702G>A|p.Glu234Glu |
S182 |
13 | BAA03g21770 | A03 | 9843209 | C | T | missense_variant | MODERATE | c.428G>A|p.Cys143Tyr |
S125 |
14 | BAA03g21770 | A03 | 9843231 | G | A | missense_variant | MODERATE | c.406C>T|p.Pro136Ser |
S289 S290 |
15 | BAA03g21770 | A03 | 9843455 | G | A | missense_variant | MODERATE | c.182C>T|p.Ser61Phe |
S282 |
16 | BAA03g21770 | A03 | 9845456 | G | A | upstream_gene_variant | MODIFIER | c.-1820C>T| |
S89 |
17 | BAA03g21770 | A03 | 9845484 | C | T | upstream_gene_variant | MODIFIER | c.-1848G>A| |
S241 |
18 | BAA03g21770 | A03 | 9847979 | G | A | upstream_gene_variant | MODIFIER | c.-4343C>T| |
S133 |