Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68980 | A09 | 61782970 | C | T | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S255 |
2 | BAA09g68980 | A09 | 61783016 | C | T | missense_variant | MODERATE | c.692C>T|p.Ser231Phe |
S50 |
3 | BAA09g68980 | A09 | 61783043 | C | T | missense_variant | MODERATE | c.719C>T|p.Ala240Val |
S136 |
4 | BAA09g68980 | A09 | 61783919 | G | A | missense_variant&splice_region_variant | MODERATE | c.1379G>A|p.Gly460Glu |
S14 |
5 | BAA09g68980 | A09 | 61784533 | G | A | intron_variant | MODIFIER | c.1528+263G>A| |
S167 |
6 | BAA09g68980 | A09 | 61786380 | C | T | missense_variant | MODERATE | c.1574C>T|p.Ser525Phe |
S11 |
7 | BAA09g68980 | A09 | 61787815 | G | A | missense_variant | MODERATE | c.2326G>A|p.Asp776Asn |
S123 |
8 | BAA09g68980 | A09 | 61788360 | G | A | missense_variant | MODERATE | c.2593G>A|p.Glu865Lys |
S195 |
9 | BAA09g68980 | A09 | 61788582 | G | A | missense_variant | MODERATE | c.2740G>A|p.Val914Ile |
S291 |
10 | BAA09g68980 | A09 | 61789214 | C | T | missense_variant | MODERATE | c.3086C>T|p.Pro1029Leu |
S228 |
11 | BAA09g68980 | A09 | 61789251 | C | T | synonymous_variant | LOW | c.3123C>T|p.Ile1041Ile |
S169 |