Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14530 | A05 | 7653171 | C | T | upstream_gene_variant | MODIFIER | c.-3733C>T| |
S58 |
2 | BAA05g14530 | A05 | 7653659 | G | A | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S112 |
3 | BAA05g14530 | A05 | 7654692 | C | T | upstream_gene_variant | MODIFIER | c.-2212C>T| |
S181 |
4 | BAA05g14530 | A05 | 7654853 | C | T | upstream_gene_variant | MODIFIER | c.-2051C>T| |
S169 |
5 | BAA05g14530 | A05 | 7657535 | C | T | missense_variant | MODERATE | c.392C>T|p.Pro131Leu |
S198 |
6 | BAA05g14530 | A05 | 7657837 | C | T | missense_variant | MODERATE | c.694C>T|p.Leu232Phe |
S73 S91 |
7 | BAA05g14530 | A05 | 7657882 | G | A | missense_variant | MODERATE | c.739G>A|p.Asp247Asn |
S179 |
8 | BAA05g14530 | A05 | 7658019 | C | T | synonymous_variant | LOW | c.876C>T|p.Leu292Leu |
S135 |
9 | BAA05g14530 | A05 | 7658039 | G | A | missense_variant | MODERATE | c.896G>A|p.Gly299Glu |
S197 |
10 | BAA05g14530 | A05 | 7658204 | C | T | missense_variant | MODERATE | c.1061C>T|p.Ala354Val |
S229 |
11 | BAA05g14530 | A05 | 7658434 | C | T | missense_variant | MODERATE | c.1291C>T|p.Pro431Ser |
S181 |
12 | BAA05g14530 | A05 | 7658437 | C | T | missense_variant | MODERATE | c.1294C>T|p.Pro432Ser |
S269 |
13 | BAA05g14530 | A05 | 7658527 | C | T | missense_variant | MODERATE | c.1384C>T|p.Pro462Ser |
S262 |
14 | BAA05g14530 | A05 | 7658854 | C | T | missense_variant | MODERATE | c.1711C>T|p.Pro571Ser |
S69 |
15 | BAA05g14530 | A05 | 7661281 | G | A | downstream_gene_variant | MODIFIER | c.*2359G>A| |
S151 |
16 | BAA05g14530 | A05 | 7661379 | G | A | downstream_gene_variant | MODIFIER | c.*2457G>A| |
S37 |
17 | BAA05g14530 | A05 | 7661494 | C | T | downstream_gene_variant | MODIFIER | c.*2572C>T| |
S130 |
18 | BAA05g14530 | A05 | 7661528 | G | A | downstream_gene_variant | MODIFIER | c.*2606G>A| |
S226 |
19 | BAA05g14530 | A05 | 7661927 | C | T | downstream_gene_variant | MODIFIER | c.*3005C>T| |
S168 |
20 | BAA05g14530 | A05 | 7663597 | C | T | downstream_gene_variant | MODIFIER | c.*4675C>T| |
S59 |
21 | BAA05g14530 | A05 | 7663740 | C | T | downstream_gene_variant | MODIFIER | c.*4818C>T| |
S162 |