Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16330 | A01 | 7912350 | C | T | synonymous_variant | LOW | c.66C>T|p.Ala22Ala |
S65 |
2 | BAA01g16330 | A01 | 7912814 | G | A | missense_variant&splice_region_variant | MODERATE | c.298G>A|p.Val100Ile |
S32 |
3 | BAA01g16330 | A01 | 7913173 | G | A | missense_variant | MODERATE | c.509G>A|p.Gly170Glu |
S181 S217 S248 |
4 | BAA01g16330 | A01 | 7913387 | G | A | missense_variant | MODERATE | c.637G>A|p.Asp213Asn |
S209 |
5 | BAA01g16330 | A01 | 7913519 | C | T | intron_variant | MODIFIER | c.660+109C>T| |
S107 |
6 | BAA01g16330 | A01 | 7913524 | C | T | intron_variant | MODIFIER | c.660+114C>T| |
S33 |
7 | BAA01g16330 | A01 | 7913809 | C | T | missense_variant | MODERATE | c.743C>T|p.Pro248Leu |
S111 |
8 | BAA01g16330 | A01 | 7914197 | C | T | intron_variant | MODIFIER | c.873+23C>T| |
S100 S82 S92 |
9 | BAA01g16330 | A01 | 7915652 | G | A | downstream_gene_variant | MODIFIER | c.*468G>A| |
S201 |
10 | BAA01g16330 | A01 | 7916522 | C | T | downstream_gene_variant | MODIFIER | c.*1338C>T| |
S182 |
11 | BAA01g16330 | A01 | 7919128 | G | A | downstream_gene_variant | MODIFIER | c.*3944G>A| |
S179 S193 |
12 | BAA01g16330 | A01 | 7919670 | C | T | downstream_gene_variant | MODIFIER | c.*4486C>T| |
S200 |