Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11360 | A07 | 20043859 | C | T | downstream_gene_variant | MODIFIER | c.*4469G>A| |
S94 |
2 | BAA07g11360 | A07 | 20044823 | C | T | downstream_gene_variant | MODIFIER | c.*3505G>A| |
S192 |
3 | BAA07g11360 | A07 | 20045751 | G | A | downstream_gene_variant | MODIFIER | c.*2577C>T| |
S14 |
4 | BAA07g11360 | A07 | 20046651 | G | A | downstream_gene_variant | MODIFIER | c.*1677C>T| |
S257 |
5 | BAA07g11360 | A07 | 20047526 | C | T | downstream_gene_variant | MODIFIER | c.*802G>A| |
S179 |
6 | BAA07g11360 | A07 | 20047937 | C | T | downstream_gene_variant | MODIFIER | c.*391G>A| |
S265 |
7 | BAA07g11360 | A07 | 20049977 | C | T | intron_variant | MODIFIER | c.1330-79G>A| |
S181 |
8 | BAA07g11360 | A07 | 20049995 | G | A | intron_variant | MODIFIER | c.1330-97C>T| |
S61 |
9 | BAA07g11360 | A07 | 20050661 | G | A | missense_variant | MODERATE | c.1129C>T|p.Leu377Phe |
S170 |
10 | BAA07g11360 | A07 | 20051630 | C | T | intron_variant | MODIFIER | c.771+43G>A| |
S152 |
11 | BAA07g11360 | A07 | 20052330 | G | A | synonymous_variant | LOW | c.391C>T|p.Leu131Leu |
S45 |
12 | BAA07g11360 | A07 | 20052666 | C | T | missense_variant | MODERATE | c.125G>A|p.Arg42Lys |
S107 |
13 | BAA07g11360 | A07 | 20052901 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S265 |
14 | BAA07g11360 | A07 | 20053041 | G | A | upstream_gene_variant | MODIFIER | c.-141C>T| |
S183 |
15 | BAA07g11360 | A07 | 20053688 | C | T | upstream_gene_variant | MODIFIER | c.-788G>A| |
S57 |
16 | BAA07g11360 | A07 | 20053821 | G | A | upstream_gene_variant | MODIFIER | c.-921C>T| |
S25 |
17 | BAA07g11360 | A07 | 20055096 | C | T | upstream_gene_variant | MODIFIER | c.-2196G>A| |
S4 |
18 | BAA07g11360 | A07 | 20056363 | C | T | upstream_gene_variant | MODIFIER | c.-3463G>A| |
S32 |
19 | BAA07g11360 | A07 | 20056458 | G | A | upstream_gene_variant | MODIFIER | c.-3558C>T| |
S302 |