Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43470 | A05 | 40839889 | C | T | synonymous_variant | LOW | c.90C>T|p.Ile30Ile |
S234 |
2 | BAA05g43470 | A05 | 40840790 | G | A | missense_variant | MODERATE | c.680G>A|p.Gly227Asp |
S20 |
3 | BAA05g43470 | A05 | 40842962 | G | A | missense_variant | MODERATE | c.2680G>A|p.Glu894Lys |
S240 |
4 | BAA05g43470 | A05 | 40843229 | G | A | splice_donor_variant&intron_variant | HIGH | c.2946+1G>A| |
S302 |
5 | BAA05g43470 | A05 | 40843802 | G | A | missense_variant | MODERATE | c.3016G>A|p.Asp1006Asn |
S279 |
6 | BAA05g43470 | A05 | 40844371 | G | A | missense_variant | MODERATE | c.3397G>A|p.Asp1133Asn |
S84 S93 |
7 | BAA05g43470 | A05 | 40845107 | G | A | splice_donor_variant&intron_variant | HIGH | c.3684+1G>A| |
S193 S304 |
8 | BAA05g43470 | A05 | 40845622 | C | T | missense_variant | MODERATE | c.3904C>T|p.Pro1302Ser |
S138 |
9 | BAA05g43470 | A05 | 40846710 | C | T | synonymous_variant | LOW | c.4632C>T|p.Pro1544Pro |
S65 |
10 | BAA05g43470 | A05 | 40846879 | C | T | synonymous_variant | LOW | c.4801C>T|p.Leu1601Leu |
S72 S78 |
11 | BAA05g43470 | A05 | 40847221 | C | T | missense_variant | MODERATE | c.5143C>T|p.Pro1715Ser |
S187 |
12 | BAA05g43470 | A05 | 40847784 | C | T | synonymous_variant | LOW | c.5706C>T|p.Asp1902Asp |
S16 |
13 | BAA05g43470 | A05 | 40848468 | G | A | missense_variant | MODERATE | c.6293G>A|p.Ser2098Asn |
S251 |
14 | BAA05g43470 | A05 | 40849673 | G | A | downstream_gene_variant | MODIFIER | c.*1066G>A| |
S225 |