Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g21740 | A04 | 24419047 | G | A | downstream_gene_variant | MODIFIER | c.*2204C>T| |
S269 |
2 | BAA04g21740 | A04 | 24421423 | C | T | missense_variant | MODERATE | c.962G>A|p.Gly321Glu |
S132 S137 S215 S89 |
3 | BAA04g21740 | A04 | 24422023 | G | A | missense_variant | MODERATE | c.620C>T|p.Ser207Leu |
S41 |
4 | BAA04g21740 | A04 | 24422051 | G | A | missense_variant | MODERATE | c.592C>T|p.Pro198Ser |
S126 |
5 | BAA04g21740 | A04 | 24422245 | G | A | missense_variant | MODERATE | c.506C>T|p.Pro169Leu |
S61 |
6 | BAA04g21740 | A04 | 24422263 | C | T | missense_variant | MODERATE | c.488G>A|p.Arg163Lys |
S81 |
7 | BAA04g21740 | A04 | 24423396 | C | T | missense_variant&splice_region_variant | MODERATE | c.284G>A|p.Gly95Glu |
S63 |
8 | BAA04g21740 | A04 | 24424514 | C | T | intron_variant | MODIFIER | c.281+426G>A| |
S132 S137 S215 S89 |
9 | BAA04g21740 | A04 | 24426061 | G | A | upstream_gene_variant | MODIFIER | c.-841C>T| |
S175 |
10 | BAA04g21740 | A04 | 24426740 | C | T | upstream_gene_variant | MODIFIER | c.-1520G>A| |
S276 |
11 | BAA04g21740 | A04 | 24427566 | C | T | upstream_gene_variant | MODIFIER | c.-2346G>A| |
S67 |
12 | BAA04g21740 | A04 | 24428068 | G | A | upstream_gene_variant | MODIFIER | c.-2848C>T| |
S158 |
13 | BAA04g21740 | A04 | 24428295 | G | A | upstream_gene_variant | MODIFIER | c.-3075C>T| |
S206 S26 |
14 | BAA04g21740 | A04 | 24428344 | G | A | upstream_gene_variant | MODIFIER | c.-3124C>T| |
S71 |
15 | BAA04g21740 | A04 | 24428361 | G | A | upstream_gene_variant | MODIFIER | c.-3141C>T| |
S280 |
16 | BAA04g21740 | A04 | 24428523 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S34 |
17 | BAA04g21740 | A04 | 24430015 | G | A | upstream_gene_variant | MODIFIER | c.-4795C>T| |
S169 |