Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31600 | A01 | 20668029 | G | A | downstream_gene_variant | MODIFIER | c.*2420C>T| |
S263 |
2 | BAA01g31600 | A01 | 20668912 | C | T | downstream_gene_variant | MODIFIER | c.*1537G>A| |
S275 |
3 | BAA01g31600 | A01 | 20669100 | G | A | downstream_gene_variant | MODIFIER | c.*1349C>T| |
S33 |
4 | BAA01g31600 | A01 | 20669652 | C | T | downstream_gene_variant | MODIFIER | c.*797G>A| |
S213 |
5 | BAA01g31600 | A01 | 20669917 | T | G | downstream_gene_variant | MODIFIER | c.*532A>C| |
S1 S90 |
6 | BAA01g31600 | A01 | 20670041 | G | A | downstream_gene_variant | MODIFIER | c.*408C>T| |
S202 |
7 | BAA01g31600 | A01 | 20670692 | G | A | synonymous_variant | LOW | c.672C>T|p.His224His |
S155 |
8 | BAA01g31600 | A01 | 20671579 | G | A | missense_variant | MODERATE | c.154C>T|p.Leu52Phe |
S15 S3 |
9 | BAA01g31600 | A01 | 20671729 | C | T | missense_variant | MODERATE | c.4G>A|p.Glu2Lys |
S266 |
10 | BAA01g31600 | A01 | 20671821 | C | T | upstream_gene_variant | MODIFIER | c.-89G>A| |
S42 |
11 | BAA01g31600 | A01 | 20671869 | G | A | upstream_gene_variant | MODIFIER | c.-137C>T| |
S149 |
12 | BAA01g31600 | A01 | 20672371 | C | T | upstream_gene_variant | MODIFIER | c.-639G>A| |
S46 |
13 | BAA01g31600 | A01 | 20672518 | G | A | upstream_gene_variant | MODIFIER | c.-786C>T| |
S288 |
14 | BAA01g31600 | A01 | 20672698 | G | A | upstream_gene_variant | MODIFIER | c.-966C>T| |
S301 S304 |
15 | BAA01g31600 | A01 | 20672709 | G | A | upstream_gene_variant | MODIFIER | c.-977C>T| |
S281 |
16 | BAA01g31600 | A01 | 20672722 | C | T | upstream_gene_variant | MODIFIER | c.-990G>A| |
S167 S80 |
17 | BAA01g31600 | A01 | 20672888 | G | A | upstream_gene_variant | MODIFIER | c.-1156C>T| |
S65 |
18 | BAA01g31600 | A01 | 20673413 | G | A | upstream_gene_variant | MODIFIER | c.-1681C>T| |
S65 |
19 | BAA01g31600 | A01 | 20673621 | G | A | upstream_gene_variant | MODIFIER | c.-1889C>T| |
S302 |
20 | BAA01g31600 | A01 | 20676147 | C | T | upstream_gene_variant | MODIFIER | c.-4415G>A| |
S235 |