Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34970 | A02 | 30087333 | C | T | upstream_gene_variant | MODIFIER | c.-2191C>T| |
S18 |
2 | BAA02g34970 | A02 | 30087376 | C | T | upstream_gene_variant | MODIFIER | c.-2148C>T| |
S203 |
3 | BAA02g34970 | A02 | 30088081 | C | T | upstream_gene_variant | MODIFIER | c.-1443C>T| |
S64 |
4 | BAA02g34970 | A02 | 30088294 | C | T | upstream_gene_variant | MODIFIER | c.-1230C>T| |
S122 |
5 | BAA02g34970 | A02 | 30088302 | G | A | upstream_gene_variant | MODIFIER | c.-1222G>A| |
S80 |
6 | BAA02g34970 | A02 | 30089593 | C | T | missense_variant | MODERATE | c.70C>T|p.Leu24Phe |
S193 |
7 | BAA02g34970 | A02 | 30089618 | C | T | missense_variant | MODERATE | c.95C>T|p.Ala32Val |
S219 |
8 | BAA02g34970 | A02 | 30090087 | C | T | synonymous_variant | LOW | c.564C>T|p.Leu188Leu |
S173 |
9 | BAA02g34970 | A02 | 30090459 | C | T | synonymous_variant | LOW | c.936C>T|p.Asn312Asn |
S139 |
10 | BAA02g34970 | A02 | 30090602 | G | A | missense_variant | MODERATE | c.1079G>A|p.Cys360Tyr |
S71 |
11 | BAA02g34970 | A02 | 30091276 | C | T | synonymous_variant | LOW | c.1539C>T|p.Ser513Ser |
S112 |
12 | BAA02g34970 | A02 | 30091808 | G | A | missense_variant | MODERATE | c.1891G>A|p.Glu631Lys |
S123 |
13 | BAA02g34970 | A02 | 30092174 | C | T | missense_variant | MODERATE | c.2257C>T|p.Pro753Ser |
S6 |
14 | BAA02g34970 | A02 | 30092383 | C | T | synonymous_variant | LOW | c.2466C>T|p.Phe822Phe |
S239 |
15 | BAA02g34970 | A02 | 30092462 | G | A | missense_variant | MODERATE | c.2545G>A|p.Ala849Thr |
S82 S92 |
16 | BAA02g34970 | A02 | 30092892 | G | A | missense_variant | MODERATE | c.2975G>A|p.Ser992Asn |
S225 |
17 | BAA02g34970 | A02 | 30094630 | G | A | downstream_gene_variant | MODIFIER | c.*1704G>A| |
S306 |