Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00900 | A07 | 615473 | C | T | upstream_gene_variant | MODIFIER | c.-4989C>T| |
S28 |
2 | BAA07g00900 | A07 | 616296 | C | T | upstream_gene_variant | MODIFIER | c.-4166C>T| |
S41 |
3 | BAA07g00900 | A07 | 616318 | G | A | upstream_gene_variant | MODIFIER | c.-4144G>A| |
S193 |
4 | BAA07g00900 | A07 | 616627 | G | A | upstream_gene_variant | MODIFIER | c.-3835G>A| |
S296 |
5 | BAA07g00900 | A07 | 616729 | G | A | upstream_gene_variant | MODIFIER | c.-3733G>A| |
S96 |
6 | BAA07g00900 | A07 | 617107 | C | T | upstream_gene_variant | MODIFIER | c.-3355C>T| |
S15 S156 S3 S4 S6 |
7 | BAA07g00900 | A07 | 617166 | G | A | upstream_gene_variant | MODIFIER | c.-3296G>A| |
S234 |
8 | BAA07g00900 | A07 | 617256 | C | T | upstream_gene_variant | MODIFIER | c.-3206C>T| |
S116 |
9 | BAA07g00900 | A07 | 621520 | C | T | missense_variant | MODERATE | c.707C>T|p.Pro236Leu |
S13 S140 S219 S278 |
10 | BAA07g00900 | A07 | 621903 | C | A | missense_variant | MODERATE | c.992C>A|p.Ala331Glu |
S55 |
11 | BAA07g00900 | A07 | 622346 | C | T | missense_variant | MODERATE | c.1231C>T|p.Pro411Ser |
S95 |
12 | BAA07g00900 | A07 | 622463 | C | T | missense_variant | MODERATE | c.1264C>T|p.Arg422Trp |
S18 |
13 | BAA07g00900 | A07 | 623361 | G | A | synonymous_variant | LOW | c.1836G>A|p.Arg612Arg |
S271 |
14 | BAA07g00900 | A07 | 624044 | G | A | synonymous_variant | LOW | c.2358G>A|p.Arg786Arg |
S294 |
15 | BAA07g00900 | A07 | 624732 | G | A | missense_variant | MODERATE | c.2819G>A|p.Gly940Glu |
S240 |
16 | BAA07g00900 | A07 | 626443 | C | T | downstream_gene_variant | MODIFIER | c.*1662C>T| |
S139 |
17 | BAA07g00900 | A07 | 627487 | C | T | downstream_gene_variant | MODIFIER | c.*2706C>T| |
S118 |