Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13070 | A09 | 7522651 | C | T | upstream_gene_variant | MODIFIER | c.-3530C>T| |
S283 |
2 | BAA09g13070 | A09 | 7524343 | C | A | upstream_gene_variant | MODIFIER | c.-1838C>A| |
S123 S153 S178 S190 S223 S255 S265 S287 S292 S308 S50 S60 S76 S95 |
3 | BAA09g13070 | A09 | 7524353 | C | A | upstream_gene_variant | MODIFIER | c.-1828C>A| |
S120 S178 S216 S223 S265 S287 S292 S301 S60 S76 S77 |
4 | BAA09g13070 | A09 | 7524904 | G | A | upstream_gene_variant | MODIFIER | c.-1277G>A| |
S67 |
5 | BAA09g13070 | A09 | 7524914 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S1 S90 |
6 | BAA09g13070 | A09 | 7525411 | C | T | upstream_gene_variant | MODIFIER | c.-770C>T| |
S272 |
7 | BAA09g13070 | A09 | 7525428 | G | A | upstream_gene_variant | MODIFIER | c.-753G>A| |
S259 |
8 | BAA09g13070 | A09 | 7526763 | C | T | missense_variant | MODERATE | c.583C>T|p.Leu195Phe |
S64 |
9 | BAA09g13070 | A09 | 7526832 | G | A | missense_variant | MODERATE | c.652G>A|p.Glu218Lys |
S151 S263 |
10 | BAA09g13070 | A09 | 7526915 | C | T | synonymous_variant | LOW | c.735C>T|p.Leu245Leu |
S6 |
11 | BAA09g13070 | A09 | 7527623 | G | A | synonymous_variant | LOW | c.1443G>A|p.Arg481Arg |
S276 |
12 | BAA09g13070 | A09 | 7527978 | G | A | missense_variant | MODERATE | c.1798G>A|p.Glu600Lys |
S271 |
13 | BAA09g13070 | A09 | 7528954 | G | A | missense_variant | MODERATE | c.2450G>A|p.Arg817Lys |
S151 S263 S266 |
14 | BAA09g13070 | A09 | 7529402 | G | A | stop_gained | HIGH | c.2898G>A|p.Trp966* |
S113 |
15 | BAA09g13070 | A09 | 7530231 | G | A | missense_variant | MODERATE | c.3502G>A|p.Glu1168Lys |
S189 |
16 | BAA09g13070 | A09 | 7530775 | G | A | missense_variant | MODERATE | c.3874G>A|p.Gly1292Ser |
S188 |
17 | BAA09g13070 | A09 | 7530965 | C | T | missense_variant | MODERATE | c.4064C>T|p.Thr1355Ile |
S269 |