Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g28930 | A09 | 19074277 | C | T | upstream_gene_variant | MODIFIER | c.-4792C>T| |
S183 S198 |
2 | BAA09g28930 | A09 | 19079356 | C | T | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S188 |
3 | BAA09g28930 | A09 | 19080082 | C | T | missense_variant | MODERATE | c.839C>T|p.Ala280Val |
S193 |
4 | BAA09g28930 | A09 | 19081818 | C | T | synonymous_variant | LOW | c.1425C>T|p.Pro475Pro |
S48 |
5 | BAA09g28930 | A09 | 19082145 | G | A | missense_variant&splice_region_variant | MODERATE | c.1649G>A|p.Ser550Asn |
S266 |
6 | BAA09g28930 | A09 | 19082225 | G | A | missense_variant | MODERATE | c.1729G>A|p.Ala577Thr |
S70 |
7 | BAA09g28930 | A09 | 19082714 | C | T | intron_variant | MODIFIER | c.1828+390C>T| |
S179 |
8 | BAA09g28930 | A09 | 19083190 | G | A | intron_variant | MODIFIER | c.1829-325G>A| |
S216 |
9 | BAA09g28930 | A09 | 19083731 | G | A | intron_variant | MODIFIER | c.1982-25G>A| |
S184 |
10 | BAA09g28930 | A09 | 19083866 | G | A | missense_variant&splice_region_variant | MODERATE | c.2092G>A|p.Glu698Lys |
S1 S280 S90 |
11 | BAA09g28930 | A09 | 19084193 | G | A | stop_gained | HIGH | c.2328G>A|p.Trp776* |
S167 |
12 | BAA09g28930 | A09 | 19084270 | G | A | missense_variant | MODERATE | c.2405G>A|p.Arg802Lys |
S229 |
13 | BAA09g28930 | A09 | 19084302 | G | A | missense_variant | MODERATE | c.2437G>A|p.Ala813Thr |
S45 |
14 | BAA09g28930 | A09 | 19084327 | C | T | missense_variant | MODERATE | c.2462C>T|p.Thr821Ile |
S263 |
15 | BAA09g28930 | A09 | 19084462 | C | T | missense_variant | MODERATE | c.2492C>T|p.Pro831Leu |
S30 S31 |
16 | BAA09g28930 | A09 | 19084527 | C | T | missense_variant | MODERATE | c.2557C>T|p.Pro853Ser |
S133 |
17 | BAA09g28930 | A09 | 19085290 | C | T | synonymous_variant | LOW | c.3135C>T|p.Leu1045Leu |
S140 |
18 | BAA09g28930 | A09 | 19085500 | G | A | synonymous_variant | LOW | c.3345G>A|p.Ala1115Ala |
S124 |
19 | BAA09g28930 | A09 | 19085883 | G | A | intron_variant | MODIFIER | c.3689+39G>A| |
S15 S3 |
20 | BAA09g28930 | A09 | 19085975 | G | A | missense_variant | MODERATE | c.3739G>A|p.Ala1247Thr |
S171 |
21 | BAA09g28930 | A09 | 19086362 | C | A | missense_variant | MODERATE | c.3969C>A|p.Asn1323Lys |
S169 |
22 | BAA09g28930 | A09 | 19086775 | G | A | missense_variant | MODERATE | c.4106G>A|p.Gly1369Glu |
S196 |
23 | BAA09g28930 | A09 | 19086999 | C | T | synonymous_variant | LOW | c.4330C>T|p.Leu1444Leu |
S95 |
24 | BAA09g28930 | A09 | 19087719 | G | A | downstream_gene_variant | MODIFIER | c.*532G>A| |
S210 S225 |
25 | BAA09g28930 | A09 | 19088038 | G | A | downstream_gene_variant | MODIFIER | c.*851G>A| |
S281 |