Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04760 | A10 | 2438405 | G | A | upstream_gene_variant | MODIFIER | c.-4369G>A| |
S219 S72 |
2 | BAA10g04760 | A10 | 2440610 | G | A | upstream_gene_variant | MODIFIER | c.-2164G>A| |
S111 |
3 | BAA10g04760 | A10 | 2440662 | G | A | upstream_gene_variant | MODIFIER | c.-2112G>A| |
S241 |
4 | BAA10g04760 | A10 | 2442832 | G | A | missense_variant | MODERATE | c.59G>A|p.Ser20Asn |
S179 |
5 | BAA10g04760 | A10 | 2443378 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S63 |
6 | BAA10g04760 | A10 | 2443921 | C | T | missense_variant | MODERATE | c.754C>T|p.Pro252Ser |
S41 |
7 | BAA10g04760 | A10 | 2443926 | G | A | synonymous_variant | LOW | c.759G>A|p.Arg253Arg |
S15 |
8 | BAA10g04760 | A10 | 2444307 | G | A | synonymous_variant | LOW | c.1140G>A|p.Gly380Gly |
S240 |
9 | BAA10g04760 | A10 | 2444390 | C | T | missense_variant | MODERATE | c.1223C>T|p.Thr408Ile |
S116 |
10 | BAA10g04760 | A10 | 2444816 | G | A | missense_variant | MODERATE | c.1649G>A|p.Gly550Asp |
S18 |
11 | BAA10g04760 | A10 | 2445523 | G | A | synonymous_variant | LOW | c.2274G>A|p.Arg758Arg |
S153 S213 |
12 | BAA10g04760 | A10 | 2447272 | G | A | missense_variant | MODERATE | c.2903G>A|p.Gly968Glu |
S160 |
13 | BAA10g04760 | A10 | 2447677 | G | A | missense_variant | MODERATE | c.3196G>A|p.Ala1066Thr |
S16 |
14 | BAA10g04760 | A10 | 2448105 | G | A | missense_variant | MODERATE | c.3514G>A|p.Gly1172Arg |
S65 |
15 | BAA10g04760 | A10 | 2448126 | C | T | missense_variant | MODERATE | c.3535C>T|p.Pro1179Ser |
S202 |
16 | BAA10g04760 | A10 | 2452340 | G | A | downstream_gene_variant | MODIFIER | c.*4155G>A| |
S215 |