Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46320 | A01 | 30891341 | C | T | splice_region_variant&stop_retained_variant | LOW | c.1733G>A|p.Ter578Ter |
S78 S83 |
2 | BAA01g46320 | A01 | 30892206 | G | A | missense_variant | MODERATE | c.1366C>T|p.Pro456Ser |
S71 |
3 | BAA01g46320 | A01 | 30893176 | A | T | intron_variant | MODIFIER | c.1264-32T>A| |
S129 |
4 | BAA01g46320 | A01 | 30893457 | C | T | missense_variant | MODERATE | c.1100G>A|p.Gly367Glu |
S177 |
5 | BAA01g46320 | A01 | 30893933 | C | T | intron_variant | MODIFIER | c.1092+281G>A| |
S13 S140 S168 S219 S279 S64 S72 |
6 | BAA01g46320 | A01 | 30894964 | G | A | intron_variant | MODIFIER | c.971-554C>T| |
S262 |
7 | BAA01g46320 | A01 | 30895170 | C | T | intron_variant | MODIFIER | c.971-760G>A| |
S266 |
8 | BAA01g46320 | A01 | 30896278 | C | T | intron_variant | MODIFIER | c.970+878G>A| |
S276 |
9 | BAA01g46320 | A01 | 30897290 | C | T | stop_gained | HIGH | c.927G>A|p.Trp309* |
S104 S52 |
10 | BAA01g46320 | A01 | 30900024 | C | T | upstream_gene_variant | MODIFIER | c.-1114G>A| |
S54 |
11 | BAA01g46320 | A01 | 30900174 | C | T | upstream_gene_variant | MODIFIER | c.-1264G>A| |
S210 S225 |
12 | BAA01g46320 | A01 | 30901370 | C | T | upstream_gene_variant | MODIFIER | c.-2460G>A| |
S4 |
13 | BAA01g46320 | A01 | 30901682 | G | A | upstream_gene_variant | MODIFIER | c.-2772C>T| |
S53 |
14 | BAA01g46320 | A01 | 30901688 | G | A | upstream_gene_variant | MODIFIER | c.-2778C>T| |
S302 |
15 | BAA01g46320 | A01 | 30903106 | G | A | upstream_gene_variant | MODIFIER | c.-4196C>T| |
S257 |
16 | BAA01g46320 | A01 | 30903250 | G | A | upstream_gene_variant | MODIFIER | c.-4340C>T| |
S169 |