Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11270 | A09 | 6332612 | G | A | missense_variant | MODERATE | c.4414C>T|p.Pro1472Ser |
S80 |
2 | BAA09g11270 | A09 | 6332841 | C | T | synonymous_variant | LOW | c.4185G>A|p.Leu1395Leu |
S284 |
3 | BAA09g11270 | A09 | 6333149 | G | A | synonymous_variant | LOW | c.3877C>T|p.Leu1293Leu |
S60 |
4 | BAA09g11270 | A09 | 6333513 | C | T | missense_variant | MODERATE | c.3607G>A|p.Asp1203Asn |
S183 |
5 | BAA09g11270 | A09 | 6334989 | C | T | synonymous_variant | LOW | c.2979G>A|p.Glu993Glu |
S275 |
6 | BAA09g11270 | A09 | 6335505 | G | A | synonymous_variant | LOW | c.2463C>T|p.Asp821Asp |
S162 S28 |
7 | BAA09g11270 | A09 | 6335525 | C | T | missense_variant&splice_region_variant | MODERATE | c.2443G>A|p.Ala815Thr |
S246 |
8 | BAA09g11270 | A09 | 6336661 | G | A | intron_variant | MODIFIER | c.2255-530C>T| |
S185 |
9 | BAA09g11270 | A09 | 6337571 | C | T | missense_variant | MODERATE | c.2002G>A|p.Glu668Lys |
S50 |
10 | BAA09g11270 | A09 | 6337750 | C | T | missense_variant | MODERATE | c.1823G>A|p.Gly608Glu |
S71 |
11 | BAA09g11270 | A09 | 6339296 | C | T | missense_variant | MODERATE | c.277G>A|p.Glu93Lys |
S298 |
12 | BAA09g11270 | A09 | 6340850 | C | T | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S155 |
13 | BAA09g11270 | A09 | 6341515 | C | T | upstream_gene_variant | MODIFIER | c.-1943G>A| |
S51 |