Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27100 | A02 | 15216109 | G | A | downstream_gene_variant | MODIFIER | c.*4179C>T| |
S264 |
2 | BAA02g27100 | A02 | 15216709 | G | A | downstream_gene_variant | MODIFIER | c.*3579C>T| |
S169 |
3 | BAA02g27100 | A02 | 15217027 | C | T | downstream_gene_variant | MODIFIER | c.*3261G>A| |
S77 S82 |
4 | BAA02g27100 | A02 | 15220590 | C | T | missense_variant | MODERATE | c.1648G>A|p.Val550Ile |
S245 |
5 | BAA02g27100 | A02 | 15220963 | A | T | missense_variant | MODERATE | c.1349T>A|p.Leu450His |
S100 |
6 | BAA02g27100 | A02 | 15221387 | G | A | splice_region_variant&intron_variant | LOW | c.931-6C>T| |
S187 |
7 | BAA02g27100 | A02 | 15221544 | C | T | missense_variant | MODERATE | c.874G>A|p.Gly292Arg |
S176 |
8 | BAA02g27100 | A02 | 15221546 | C | T | missense_variant | MODERATE | c.872G>A|p.Ser291Asn |
S107 |
9 | BAA02g27100 | A02 | 15221643 | C | T | missense_variant | MODERATE | c.775G>A|p.Glu259Lys |
S202 |
10 | BAA02g27100 | A02 | 15221754 | G | A | missense_variant | MODERATE | c.719C>T|p.Ala240Val |
S155 S211 |
11 | BAA02g27100 | A02 | 15222657 | C | T | missense_variant | MODERATE | c.361G>A|p.Glu121Lys |
S25 S264 |
12 | BAA02g27100 | A02 | 15223140 | G | A | upstream_gene_variant | MODIFIER | c.-123C>T| |
S23 |
13 | BAA02g27100 | A02 | 15223150 | G | A | upstream_gene_variant | MODIFIER | c.-133C>T| |
S229 |
14 | BAA02g27100 | A02 | 15223567 | G | A | upstream_gene_variant | MODIFIER | c.-550C>T| |
S47 |
15 | BAA02g27100 | A02 | 15224106 | C | T | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S94 |
16 | BAA02g27100 | A02 | 15225066 | G | A | upstream_gene_variant | MODIFIER | c.-2049C>T| |
S186 |
17 | BAA02g27100 | A02 | 15226552 | G | A | upstream_gene_variant | MODIFIER | c.-3535C>T| |
S265 |
18 | BAA02g27100 | A02 | 15227292 | G | A | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S60 |