Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g14600 | A04 | 19596466 | G | A | downstream_gene_variant | MODIFIER | c.*3788C>T| |
S190 |
2 | BAA04g14600 | A04 | 19596599 | G | A | downstream_gene_variant | MODIFIER | c.*3655C>T| |
S62 |
3 | BAA04g14600 | A04 | 19596632 | C | T | downstream_gene_variant | MODIFIER | c.*3622G>A| |
S209 |
4 | BAA04g14600 | A04 | 19597059 | G | A | downstream_gene_variant | MODIFIER | c.*3195C>T| |
S194 |
5 | BAA04g14600 | A04 | 19599846 | C | T | downstream_gene_variant | MODIFIER | c.*408G>A| |
S250 |
6 | BAA04g14600 | A04 | 19600035 | C | T | downstream_gene_variant | MODIFIER | c.*219G>A| |
S46 |
7 | BAA04g14600 | A04 | 19600786 | G | A | missense_variant | MODERATE | c.1430C>T|p.Ser477Phe |
S295 |
8 | BAA04g14600 | A04 | 19601320 | C | T | synonymous_variant | LOW | c.1005G>A|p.Leu335Leu |
S212 |
9 | BAA04g14600 | A04 | 19601679 | G | A | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S181 |
10 | BAA04g14600 | A04 | 19601816 | C | T | missense_variant | MODERATE | c.509G>A|p.Cys170Tyr |
S6 |
11 | BAA04g14600 | A04 | 19601942 | C | T | missense_variant | MODERATE | c.383G>A|p.Arg128His |
S252 |
12 | BAA04g14600 | A04 | 19602114 | C | T | missense_variant | MODERATE | c.211G>A|p.Glu71Lys |
S270 |
13 | BAA04g14600 | A04 | 19604191 | C | T | upstream_gene_variant | MODIFIER | c.-1867G>A| |
S152 |
14 | BAA04g14600 | A04 | 19606122 | G | A | upstream_gene_variant | MODIFIER | c.-3798C>T| |
S202 |
15 | BAA04g14600 | A04 | 19606511 | G | A | upstream_gene_variant | MODIFIER | c.-4187C>T| |
S259 |
16 | BAA04g14600 | A04 | 19606546 | C | T | upstream_gene_variant | MODIFIER | c.-4222G>A| |
S20 |
17 | BAA04g14600 | A04 | 19606579 | C | T | upstream_gene_variant | MODIFIER | c.-4255G>A| |
S139 |
18 | BAA04g14600 | A04 | 19606785 | C | T | upstream_gene_variant | MODIFIER | c.-4461G>A| |
S55 |
19 | BAA04g14600 | A04 | 19606820 | C | T | upstream_gene_variant | MODIFIER | c.-4496G>A| |
S6 |