Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09820 | A10 | 11671919 | C | T | missense_variant | MODERATE | c.2418G>A|p.Met806Ile |
S259 |
2 | BAA10g09820 | A10 | 11672158 | C | T | missense_variant | MODERATE | c.2179G>A|p.Glu727Lys |
S237 |
3 | BAA10g09820 | A10 | 11672677 | G | A | synonymous_variant | LOW | c.1738C>T|p.Leu580Leu |
S241 |
4 | BAA10g09820 | A10 | 11673357 | G | A | synonymous_variant | LOW | c.1182C>T|p.Ala394Ala |
S305 |
5 | BAA10g09820 | A10 | 11673455 | G | A | missense_variant | MODERATE | c.1084C>T|p.Leu362Phe |
S293 |
6 | BAA10g09820 | A10 | 11673464 | G | A | missense_variant | MODERATE | c.1075C>T|p.Leu359Phe |
S241 |
7 | BAA10g09820 | A10 | 11674395 | G | A | missense_variant | MODERATE | c.634C>T|p.Arg212Trp |
S289 |
8 | BAA10g09820 | A10 | 11674598 | G | A | missense_variant | MODERATE | c.509C>T|p.Ala170Val |
S43 S96 |
9 | BAA10g09820 | A10 | 11675274 | G | A | synonymous_variant | LOW | c.261C>T|p.Ala87Ala |
S292 |
10 | BAA10g09820 | A10 | 11675423 | C | T | missense_variant | MODERATE | c.112G>A|p.Asp38Asn |
S244 |