Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42370 | A09 | 48796851 | C | T | upstream_gene_variant | MODIFIER | c.-642C>T| |
S182 |
2 | BAA09g42370 | A09 | 48797037 | C | T | upstream_gene_variant | MODIFIER | c.-456C>T| |
S63 |
3 | BAA09g42370 | A09 | 48797180 | G | T | upstream_gene_variant | MODIFIER | c.-313G>T| |
S150 |
4 | BAA09g42370 | A09 | 48797609 | G | A | intron_variant | MODIFIER | c.78+39G>A| |
S107 |
5 | BAA09g42370 | A09 | 48797627 | G | A | intron_variant | MODIFIER | c.79-47G>A| |
S249 |
6 | BAA09g42370 | A09 | 48797708 | C | T | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S169 |
7 | BAA09g42370 | A09 | 48798998 | G | A | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S207 |
8 | BAA09g42370 | A09 | 48799439 | G | A | missense_variant | MODERATE | c.1525G>A|p.Asp509Asn |
S171 |
9 | BAA09g42370 | A09 | 48799664 | G | A | missense_variant | MODERATE | c.1750G>A|p.Glu584Lys |
S9 |
10 | BAA09g42370 | A09 | 48799958 | G | A | missense_variant | MODERATE | c.2044G>A|p.Gly682Ser |
S1 S90 |
11 | BAA09g42370 | A09 | 48799991 | C | T | missense_variant | MODERATE | c.2077C>T|p.Leu693Phe |
S219 S72 |
12 | BAA09g42370 | A09 | 48800039 | G | A | missense_variant | MODERATE | c.2125G>A|p.Glu709Lys |
S148 S210 |
13 | BAA09g42370 | A09 | 48800076 | C | T | missense_variant | MODERATE | c.2162C>T|p.Ser721Leu |
S159 S243 S299 |
14 | BAA09g42370 | A09 | 48800266 | G | A | stop_gained | HIGH | c.2352G>A|p.Trp784* |
S67 |
15 | BAA09g42370 | A09 | 48801705 | C | T | missense_variant | MODERATE | c.3791C>T|p.Ser1264Phe |
S293 |
16 | BAA09g42370 | A09 | 48801890 | G | A | missense_variant | MODERATE | c.3976G>A|p.Glu1326Lys |
S265 |
17 | BAA09g42370 | A09 | 48801932 | C | T | missense_variant | MODERATE | c.4018C>T|p.Leu1340Phe |
S260 |
18 | BAA09g42370 | A09 | 48802817 | G | A | missense_variant | MODERATE | c.4903G>A|p.Glu1635Lys |
S308 |
19 | BAA09g42370 | A09 | 48804505 | C | T | downstream_gene_variant | MODIFIER | c.*521C>T| |
S297 |
20 | BAA09g42370 | A09 | 48805022 | C | T | downstream_gene_variant | MODIFIER | c.*1038C>T| |
S293 |