Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14660 | A05 | 7738510 | G | A | missense_variant | MODERATE | c.2501C>T|p.Pro834Leu |
S294 |
2 | BAA05g14660 | A05 | 7738524 | C | T | synonymous_variant | LOW | c.2487G>A|p.Arg829Arg |
S51 |
3 | BAA05g14660 | A05 | 7738550 | C | T | missense_variant | MODERATE | c.2461G>A|p.Gly821Ser |
S143 |
4 | BAA05g14660 | A05 | 7738592 | T | G | synonymous_variant | LOW | c.2419A>C|p.Arg807Arg |
S124 S126 S223 S286 S287 S57 S59 S60 |
5 | BAA05g14660 | A05 | 7738618 | C | T | missense_variant | MODERATE | c.2393G>A|p.Arg798His |
S198 |
6 | BAA05g14660 | A05 | 7738792 | C | T | intron_variant | MODIFIER | c.2364+16G>A| |
S162 |
7 | BAA05g14660 | A05 | 7739469 | G | A | missense_variant | MODERATE | c.1979C>T|p.Pro660Leu |
S180 |
8 | BAA05g14660 | A05 | 7739992 | C | T | synonymous_variant | LOW | c.1605G>A|p.Lys535Lys |
S81 S85 |
9 | BAA05g14660 | A05 | 7740077 | G | A | missense_variant | MODERATE | c.1520C>T|p.Pro507Leu |
S150 |
10 | BAA05g14660 | A05 | 7740410 | G | A | missense_variant | MODERATE | c.1187C>T|p.Thr396Ile |
S262 |
11 | BAA05g14660 | A05 | 7740524 | G | A | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S62 |
12 | BAA05g14660 | A05 | 7740832 | C | T | synonymous_variant | LOW | c.765G>A|p.Lys255Lys |
S265 |
13 | BAA05g14660 | A05 | 7741524 | G | A | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S208 S219 |
14 | BAA05g14660 | A05 | 7742182 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S3 |
15 | BAA05g14660 | A05 | 7742682 | C | T | upstream_gene_variant | MODIFIER | c.-1086G>A| |
S135 |
16 | BAA05g14660 | A05 | 7744004 | C | T | upstream_gene_variant | MODIFIER | c.-2408G>A| |
S130 |
17 | BAA05g14660 | A05 | 7744805 | C | T | upstream_gene_variant | MODIFIER | c.-3209G>A| |
S267 |
18 | BAA05g14660 | A05 | 7745781 | G | A | upstream_gene_variant | MODIFIER | c.-4185C>T| |
S252 |
19 | BAA05g14660 | A05 | 7745792 | G | A | upstream_gene_variant | MODIFIER | c.-4196C>T| |
S194 |