Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45140 | A01 | 30073993 | C | T | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S260 |
2 | BAA01g45140 | A01 | 30074272 | C | T | missense_variant | MODERATE | c.1115G>A|p.Gly372Glu |
S42 |
3 | BAA01g45140 | A01 | 30074545 | C | T | missense_variant | MODERATE | c.842G>A|p.Gly281Glu |
S282 |
4 | BAA01g45140 | A01 | 30074912 | G | A | missense_variant | MODERATE | c.475C>T|p.Pro159Ser |
S224 |
5 | BAA01g45140 | A01 | 30075224 | C | T | missense_variant | MODERATE | c.163G>A|p.Val55Ile |
S120 |
6 | BAA01g45140 | A01 | 30075260 | C | T | missense_variant | MODERATE | c.127G>A|p.Asp43Asn |
S231 |
7 | BAA01g45140 | A01 | 30076508 | C | T | upstream_gene_variant | MODIFIER | c.-630G>A| |
S169 |
8 | BAA01g45140 | A01 | 30076608 | C | T | upstream_gene_variant | MODIFIER | c.-730G>A| |
S186 |
9 | BAA01g45140 | A01 | 30076699 | C | T | upstream_gene_variant | MODIFIER | c.-821G>A| |
S162 |
10 | BAA01g45140 | A01 | 30076888 | G | T | upstream_gene_variant | MODIFIER | c.-1010C>A| |
S187 S243 S276 S299 |
11 | BAA01g45140 | A01 | 30077117 | C | T | upstream_gene_variant | MODIFIER | c.-1239G>A| |
S206 S26 |
12 | BAA01g45140 | A01 | 30077353 | C | T | upstream_gene_variant | MODIFIER | c.-1475G>A| |
S260 |
13 | BAA01g45140 | A01 | 30078494 | C | T | upstream_gene_variant | MODIFIER | c.-2616G>A| |
S249 |
14 | BAA01g45140 | A01 | 30079658 | C | T | upstream_gene_variant | MODIFIER | c.-3780G>A| |
S267 |
15 | BAA01g45140 | A01 | 30079992 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S136 S296 |
16 | BAA01g45140 | A01 | 30080278 | C | T | upstream_gene_variant | MODIFIER | c.-4400G>A| |
S73 S91 |
17 | BAA01g45140 | A01 | 30080737 | G | A | upstream_gene_variant | MODIFIER | c.-4859C>T| |
S207 |