Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01260 | A04 | 706634 | C | T | missense_variant | MODERATE | c.3688G>A|p.Asp1230Asn |
S8 |
2 | BAA04g01260 | A04 | 706877 | C | T | missense_variant | MODERATE | c.3445G>A|p.Val1149Ile |
S308 |
3 | BAA04g01260 | A04 | 706880 | G | A | missense_variant | MODERATE | c.3442C>T|p.Leu1148Phe |
S232 |
4 | BAA04g01260 | A04 | 707529 | G | A | synonymous_variant | LOW | c.2793C>T|p.Asn931Asn |
S60 |
5 | BAA04g01260 | A04 | 707741 | C | T | missense_variant | MODERATE | c.2581G>A|p.Ala861Thr |
S249 S262 |
6 | BAA04g01260 | A04 | 708479 | G | A | missense_variant | MODERATE | c.1843C>T|p.Pro615Ser |
S36 |
7 | BAA04g01260 | A04 | 711531 | C | T | upstream_gene_variant | MODIFIER | c.-195G>A| |
S231 |
8 | BAA04g01260 | A04 | 711636 | G | T | upstream_gene_variant | MODIFIER | c.-300C>A| |
S143 S193 S299 |
9 | BAA04g01260 | A04 | 712070 | G | A | upstream_gene_variant | MODIFIER | c.-734C>T| |
S305 |
10 | BAA04g01260 | A04 | 712457 | G | A | upstream_gene_variant | MODIFIER | c.-1121C>T| |
S274 |
11 | BAA04g01260 | A04 | 712722 | G | A | upstream_gene_variant | MODIFIER | c.-1386C>T| |
S303 |
12 | BAA04g01260 | A04 | 712838 | T | G | upstream_gene_variant | MODIFIER | c.-1502A>C| |
S12 |
13 | BAA04g01260 | A04 | 714029 | C | T | upstream_gene_variant | MODIFIER | c.-2693G>A| |
S174 S27 |
14 | BAA04g01260 | A04 | 714393 | G | A | upstream_gene_variant | MODIFIER | c.-3057C>T| |
S276 |
15 | BAA04g01260 | A04 | 714641 | C | A | upstream_gene_variant | MODIFIER | c.-3305G>T| |
S204 S274 |
16 | BAA04g01260 | A04 | 714721 | G | T | upstream_gene_variant | MODIFIER | c.-3385C>A| |
S222 S227 S258 S75 |