Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g35180 | A05 | 35947548 | C | T | missense_variant | MODERATE | c.110C>T|p.Ser37Phe |
S59 |
2 | BAA05g35180 | A05 | 35947755 | G | A | missense_variant | MODERATE | c.248G>A|p.Arg83Lys |
S192 |
3 | BAA05g35180 | A05 | 35950389 | C | T | missense_variant | MODERATE | c.1222C>T|p.Arg408Cys |
S167 |
4 | BAA05g35180 | A05 | 35951131 | G | A | missense_variant | MODERATE | c.1604G>A|p.Gly535Glu |
S75 S81 |
5 | BAA05g35180 | A05 | 35951911 | G | A | intron_variant | MODIFIER | c.1812-24G>A| |
S197 |
6 | BAA05g35180 | A05 | 35952037 | G | A | synonymous_variant | LOW | c.1914G>A|p.Arg638Arg |
S250 |
7 | BAA05g35180 | A05 | 35952844 | G | A | splice_region_variant&intron_variant | LOW | c.2265+5G>A| |
S251 |
8 | BAA05g35180 | A05 | 35953313 | G | A | synonymous_variant | LOW | c.2463G>A|p.Gln821Gln |
S163 |
9 | BAA05g35180 | A05 | 35953932 | C | T | missense_variant | MODERATE | c.2831C>T|p.Ser944Phe |
S35 |
10 | BAA05g35180 | A05 | 35954468 | C | T | intron_variant | MODIFIER | c.3024-120C>T| |
S8 |
11 | BAA05g35180 | A05 | 35954604 | G | A | missense_variant | MODERATE | c.3040G>A|p.Glu1014Lys |
S156 S282 |
12 | BAA05g35180 | A05 | 35956052 | G | A | synonymous_variant | LOW | c.3654G>A|p.Arg1218Arg |
S231 |
13 | BAA05g35180 | A05 | 35957131 | G | A | missense_variant | MODERATE | c.4384G>A|p.Val1462Ile |
S301 S304 |
14 | BAA05g35180 | A05 | 35958695 | C | G | synonymous_variant | LOW | c.5265C>G|p.Leu1755Leu |
S143 |
15 | BAA05g35180 | A05 | 35959053 | G | A | missense_variant | MODERATE | c.5537G>A|p.Arg1846Lys |
S27 |
16 | BAA05g35180 | A05 | 35959505 | C | T | downstream_gene_variant | MODIFIER | c.*22C>T| |
S155 S211 |