Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13920 | A01 | 6612728 | G | A | downstream_gene_variant | MODIFIER | c.*3304C>T| |
S202 |
2 | BAA01g13920 | A01 | 6613026 | G | A | downstream_gene_variant | MODIFIER | c.*3006C>T| |
S243 |
3 | BAA01g13920 | A01 | 6613226 | G | A | downstream_gene_variant | MODIFIER | c.*2806C>T| |
S180 |
4 | BAA01g13920 | A01 | 6613885 | C | T | downstream_gene_variant | MODIFIER | c.*2147G>A| |
S20 |
5 | BAA01g13920 | A01 | 6615408 | C | T | downstream_gene_variant | MODIFIER | c.*624G>A| |
S302 |
6 | BAA01g13920 | A01 | 6617647 | C | T | intron_variant | MODIFIER | c.960+1103G>A| |
S42 |
7 | BAA01g13920 | A01 | 6619339 | C | T | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S249 |
8 | BAA01g13920 | A01 | 6619376 | C | T | synonymous_variant | LOW | c.534G>A|p.Arg178Arg |
S167 |
9 | BAA01g13920 | A01 | 6619398 | G | A | missense_variant | MODERATE | c.512C>T|p.Pro171Leu |
S202 |
10 | BAA01g13920 | A01 | 6619720 | C | T | missense_variant | MODERATE | c.190G>A|p.Asp64Asn |
S278 |
11 | BAA01g13920 | A01 | 6619743 | G | A | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S161 |
12 | BAA01g13920 | A01 | 6621301 | C | T | upstream_gene_variant | MODIFIER | c.-1392G>A| |
S107 |
13 | BAA01g13920 | A01 | 6621408 | C | T | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S170 |
14 | BAA01g13920 | A01 | 6621577 | G | A | upstream_gene_variant | MODIFIER | c.-1668C>T| |
S157 |
15 | BAA01g13920 | A01 | 6622029 | C | T | upstream_gene_variant | MODIFIER | c.-2120G>A| |
S196 |
16 | BAA01g13920 | A01 | 6622288 | C | T | upstream_gene_variant | MODIFIER | c.-2379G>A| |
S242 |
17 | BAA01g13920 | A01 | 6622303 | G | A | upstream_gene_variant | MODIFIER | c.-2394C>T| |
S191 |
18 | BAA01g13920 | A01 | 6622645 | C | T | upstream_gene_variant | MODIFIER | c.-2736G>A| |
S261 |