Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g45670 | A06 | 29101047 | G | A | missense_variant | MODERATE | c.1892C>T|p.Pro631Leu |
S152 |
2 | BAA06g45670 | A06 | 29101154 | C | T | synonymous_variant | LOW | c.1785G>A|p.Leu595Leu |
S301 S304 |
3 | BAA06g45670 | A06 | 29101324 | G | A | synonymous_variant | LOW | c.1696C>T|p.Leu566Leu |
S169 |
4 | BAA06g45670 | A06 | 29101729 | C | T | synonymous_variant | LOW | c.1482G>A|p.Glu494Glu |
S274 |
5 | BAA06g45670 | A06 | 29102053 | G | A | missense_variant | MODERATE | c.1396C>T|p.Leu466Phe |
S10 |
6 | BAA06g45670 | A06 | 29102675 | C | T | missense_variant | MODERATE | c.1060G>A|p.Glu354Lys |
S20 |
7 | BAA06g45670 | A06 | 29102816 | G | A | missense_variant | MODERATE | c.1010C>T|p.Ala337Val |
S261 |
8 | BAA06g45670 | A06 | 29103221 | G | A | splice_region_variant&synonymous_variant | LOW | c.774C>T|p.Arg258Arg |
S118 |
9 | BAA06g45670 | A06 | 29103447 | C | T | missense_variant | MODERATE | c.548G>A|p.Gly183Glu |
S172 S217 |
10 | BAA06g45670 | A06 | 29104057 | C | T | missense_variant | MODERATE | c.190G>A|p.Ala64Thr |
S179 |
11 | BAA06g45670 | A06 | 29105211 | G | A | upstream_gene_variant | MODIFIER | c.-965C>T| |
S33 |
12 | BAA06g45670 | A06 | 29105324 | G | A | upstream_gene_variant | MODIFIER | c.-1078C>T| |
S171 |
13 | BAA06g45670 | A06 | 29107365 | G | A | upstream_gene_variant | MODIFIER | c.-3119C>T| |
S38 |
14 | BAA06g45670 | A06 | 29107846 | C | T | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S202 |