Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44910 | A09 | 50314886 | G | A | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S292 |
2 | BAA09g44910 | A09 | 50317068 | G | A | synonymous_variant | LOW | c.405G>A|p.Leu135Leu |
S34 |
3 | BAA09g44910 | A09 | 50317393 | G | A | missense_variant&splice_region_variant | MODERATE | c.647G>A|p.Gly216Glu |
S134 |
4 | BAA09g44910 | A09 | 50318798 | C | T | stop_gained | HIGH | c.1225C>T|p.Gln409* |
S115 |
5 | BAA09g44910 | A09 | 50318930 | G | A | missense_variant | MODERATE | c.1247G>A|p.Arg416Lys |
S305 |
6 | BAA09g44910 | A09 | 50318955 | C | T | synonymous_variant | LOW | c.1272C>T|p.Asp424Asp |
S205 |
7 | BAA09g44910 | A09 | 50320296 | G | A | missense_variant | MODERATE | c.2093G>A|p.Ser698Asn |
S308 |
8 | BAA09g44910 | A09 | 50320967 | G | A | missense_variant | MODERATE | c.2450G>A|p.Arg817His |
S202 |
9 | BAA09g44910 | A09 | 50321096 | G | A | stop_gained | HIGH | c.2499G>A|p.Trp833* |
S167 |
10 | BAA09g44910 | A09 | 50321952 | C | T | synonymous_variant | LOW | c.2871C>T|p.Gly957Gly |
S114 |
11 | BAA09g44910 | A09 | 50322200 | C | T | splice_region_variant&intron_variant | LOW | c.3025-7C>T| |
S183 S198 |
12 | BAA09g44910 | A09 | 50322229 | C | T | missense_variant | MODERATE | c.3047C>T|p.Thr1016Met |
S81 S85 |
13 | BAA09g44910 | A09 | 50323284 | C | T | missense_variant | MODERATE | c.3566C>T|p.Thr1189Ile |
S108 |
14 | BAA09g44910 | A09 | 50323562 | C | T | synonymous_variant | LOW | c.3745C>T|p.Leu1249Leu |
S169 |
15 | BAA09g44910 | A09 | 50323635 | G | A | missense_variant | MODERATE | c.3818G>A|p.Arg1273Lys |
S162 |
16 | BAA09g44910 | A09 | 50323739 | C | T | synonymous_variant | LOW | c.3922C>T|p.Leu1308Leu |
S184 |
17 | BAA09g44910 | A09 | 50323803 | C | T | missense_variant | MODERATE | c.3986C>T|p.Ala1329Val |
S174 S175 |
18 | BAA09g44910 | A09 | 50323858 | G | A | synonymous_variant | LOW | c.4041G>A|p.Val1347Val |
S16 |