Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40360 | A06 | 26289465 | C | T | missense_variant | MODERATE | c.2665G>A|p.Gly889Ser |
S36 |
2 | BAA06g40360 | A06 | 26289471 | C | T | missense_variant | MODERATE | c.2659G>A|p.Glu887Lys |
S272 |
3 | BAA06g40360 | A06 | 26289647 | C | T | synonymous_variant | LOW | c.2577G>A|p.Lys859Lys |
S153 |
4 | BAA06g40360 | A06 | 26290350 | G | A | missense_variant | MODERATE | c.1945C>T|p.Pro649Ser |
S245 |
5 | BAA06g40360 | A06 | 26290575 | C | T | missense_variant | MODERATE | c.1720G>A|p.Asp574Asn |
S252 |
6 | BAA06g40360 | A06 | 26290904 | C | A | missense_variant | MODERATE | c.1391G>T|p.Gly464Val |
S266 |
7 | BAA06g40360 | A06 | 26290947 | C | T | missense_variant | MODERATE | c.1348G>A|p.Asp450Asn |
S148 S30 S31 |
8 | BAA06g40360 | A06 | 26291197 | T | G | synonymous_variant | LOW | c.1098A>C|p.Ser366Ser |
S165 S193 S290 |
9 | BAA06g40360 | A06 | 26292082 | C | T | synonymous_variant | LOW | c.618G>A|p.Ala206Ala |
S295 |
10 | BAA06g40360 | A06 | 26292771 | G | A | synonymous_variant | LOW | c.87C>T|p.Ser29Ser |
S204 |
11 | BAA06g40360 | A06 | 26295612 | C | T | upstream_gene_variant | MODIFIER | c.-2755G>A| |
S132 S137 S215 |
12 | BAA06g40360 | A06 | 26295707 | G | A | upstream_gene_variant | MODIFIER | c.-2850C>T| |
S288 |
13 | BAA06g40360 | A06 | 26295736 | C | A | upstream_gene_variant | MODIFIER | c.-2879G>T| |
S4 |
14 | BAA06g40360 | A06 | 26297025 | G | A | upstream_gene_variant | MODIFIER | c.-4168C>T| |
S129 |