Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07340 | A10 | 4200935 | G | A | missense_variant&splice_region_variant | MODERATE | c.2759C>T|p.Ala920Val |
S198 |
2 | BAA10g07340 | A10 | 4201971 | C | T | missense_variant | MODERATE | c.2227G>A|p.Asp743Asn |
S116 |
3 | BAA10g07340 | A10 | 4202172 | C | T | missense_variant | MODERATE | c.2108G>A|p.Arg703Lys |
S44 |
4 | BAA10g07340 | A10 | 4203351 | C | T | synonymous_variant | LOW | c.1377G>A|p.Glu459Glu |
S235 |
5 | BAA10g07340 | A10 | 4203561 | G | A | synonymous_variant | LOW | c.1323C>T|p.Pro441Pro |
S251 |
6 | BAA10g07340 | A10 | 4203779 | C | T | missense_variant | MODERATE | c.1207G>A|p.Gly403Arg |
S35 |
7 | BAA10g07340 | A10 | 4203824 | C | T | missense_variant | MODERATE | c.1162G>A|p.Gly388Arg |
S188 |
8 | BAA10g07340 | A10 | 4205458 | C | T | intron_variant | MODIFIER | c.1149+663G>A| |
S84 S93 |
9 | BAA10g07340 | A10 | 4205678 | G | A | intron_variant | MODIFIER | c.1149+443C>T| |
S161 |
10 | BAA10g07340 | A10 | 4206144 | G | A | synonymous_variant | LOW | c.1126C>T|p.Leu376Leu |
S18 |
11 | BAA10g07340 | A10 | 4207277 | G | A | intron_variant | MODIFIER | c.1014-1021C>T| |
S129 |
12 | BAA10g07340 | A10 | 4208379 | G | A | intron_variant | MODIFIER | c.1014-2123C>T| |
S125 |
13 | BAA10g07340 | A10 | 4210557 | C | T | intron_variant | MODIFIER | c.1013+3888G>A| |
S35 |
14 | BAA10g07340 | A10 | 4211177 | G | A | intron_variant | MODIFIER | c.1013+3268C>T| |
S57 |
15 | BAA10g07340 | A10 | 4213866 | G | A | intron_variant | MODIFIER | c.1013+579C>T| |
S295 |
16 | BAA10g07340 | A10 | 4213987 | C | T | intron_variant | MODIFIER | c.1013+458G>A| |
S199 |
17 | BAA10g07340 | A10 | 4214495 | G | A | synonymous_variant | LOW | c.963C>T|p.Leu321Leu |
S13 S140 S219 S278 S64 S72 |
18 | BAA10g07340 | A10 | 4214533 | C | T | missense_variant | MODERATE | c.925G>A|p.Glu309Lys |
S132 S137 S215 |
19 | BAA10g07340 | A10 | 4215139 | T | C | missense_variant | MODERATE | c.613A>G|p.Thr205Ala |
S53 |
20 | BAA10g07340 | A10 | 4215345 | G | A | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S36 |
21 | BAA10g07340 | A10 | 4216086 | G | A | missense_variant | MODERATE | c.49C>T|p.Pro17Ser |
S286 |
22 | BAA10g07340 | A10 | 4216919 | C | T | upstream_gene_variant | MODIFIER | c.-785G>A| |
S205 |
23 | BAA10g07340 | A10 | 4217451 | C | T | upstream_gene_variant | MODIFIER | c.-1317G>A| |
S177 |
24 | BAA10g07340 | A10 | 4217895 | G | A | upstream_gene_variant | MODIFIER | c.-1761C>T| |
S33 |
25 | BAA10g07340 | A10 | 4217991 | C | T | upstream_gene_variant | MODIFIER | c.-1857G>A| |
S51 |