Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g29000 | A06 | 19790898 | G | A | upstream_gene_variant | MODIFIER | c.-125G>A| |
S194 |
2 | BAA06g29000 | A06 | 19791178 | C | T | synonymous_variant | LOW | c.156C>T|p.Gly52Gly |
S126 |
3 | BAA06g29000 | A06 | 19791214 | G | A | synonymous_variant | LOW | c.192G>A|p.Lys64Lys |
S261 |
4 | BAA06g29000 | A06 | 19791561 | C | T | missense_variant | MODERATE | c.539C>T|p.Pro180Leu |
S279 |
5 | BAA06g29000 | A06 | 19792045 | C | T | synonymous_variant | LOW | c.873C>T|p.Tyr291Tyr |
S291 |
6 | BAA06g29000 | A06 | 19793037 | C | T | synonymous_variant | LOW | c.1695C>T|p.Leu565Leu |
S36 |
7 | BAA06g29000 | A06 | 19793443 | C | T | missense_variant | MODERATE | c.2101C>T|p.Leu701Phe |
S294 |
8 | BAA06g29000 | A06 | 19793472 | G | A | synonymous_variant | LOW | c.2130G>A|p.Lys710Lys |
S152 |
9 | BAA06g29000 | A06 | 19793488 | C | T | missense_variant | MODERATE | c.2146C>T|p.Pro716Ser |
S269 |
10 | BAA06g29000 | A06 | 19793948 | G | A | missense_variant | MODERATE | c.2498G>A|p.Gly833Asp |
S33 |
11 | BAA06g29000 | A06 | 19793979 | C | T | synonymous_variant | LOW | c.2529C>T|p.Leu843Leu |
S282 |
12 | BAA06g29000 | A06 | 19794651 | C | T | missense_variant | MODERATE | c.3049C>T|p.Leu1017Phe |
S9 |
13 | BAA06g29000 | A06 | 19795004 | G | A | synonymous_variant | LOW | c.3312G>A|p.Lys1104Lys |
S74 |
14 | BAA06g29000 | A06 | 19795341 | C | T | missense_variant | MODERATE | c.3649C>T|p.Pro1217Ser |
S256 |
15 | BAA06g29000 | A06 | 19795376 | G | A | synonymous_variant | LOW | c.3684G>A|p.Lys1228Lys |
S54 |
16 | BAA06g29000 | A06 | 19796753 | C | T | downstream_gene_variant | MODIFIER | c.*1140C>T| |
S275 |