Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23360 | A10 | 19683370 | G | A | missense_variant | MODERATE | c.5260C>T|p.Pro1754Ser |
S252 |
2 | BAA10g23360 | A10 | 19683417 | C | T | missense_variant | MODERATE | c.5213G>A|p.Ser1738Asn |
S5 |
3 | BAA10g23360 | A10 | 19685436 | C | T | missense_variant | MODERATE | c.4267G>A|p.Glu1423Lys |
S41 |
4 | BAA10g23360 | A10 | 19685910 | C | T | missense_variant | MODERATE | c.3887G>A|p.Arg1296Lys |
S124 |
5 | BAA10g23360 | A10 | 19686884 | C | T | synonymous_variant | LOW | c.2913G>A|p.Val971Val |
S296 |
6 | BAA10g23360 | A10 | 19687123 | C | T | missense_variant | MODERATE | c.2674G>A|p.Asp892Asn |
S206 S26 |
7 | BAA10g23360 | A10 | 19687467 | G | A | missense_variant | MODERATE | c.2330C>T|p.Ala777Val |
S82 S92 |
8 | BAA10g23360 | A10 | 19688107 | C | T | missense_variant | MODERATE | c.1786G>A|p.Val596Ile |
S224 |
9 | BAA10g23360 | A10 | 19688185 | C | T | missense_variant | MODERATE | c.1708G>A|p.Asp570Asn |
S91 |
10 | BAA10g23360 | A10 | 19688368 | G | A | stop_gained | HIGH | c.1525C>T|p.Gln509* |
S203 |
11 | BAA10g23360 | A10 | 19688436 | G | A | missense_variant | MODERATE | c.1457C>T|p.Pro486Leu |
S245 |
12 | BAA10g23360 | A10 | 19689064 | G | A | missense_variant | MODERATE | c.1289C>T|p.Pro430Leu |
S118 |
13 | BAA10g23360 | A10 | 19690530 | C | T | missense_variant | MODERATE | c.503G>A|p.Arg168Lys |
S133 S202 |
14 | BAA10g23360 | A10 | 19690694 | C | T | synonymous_variant | LOW | c.339G>A|p.Glu113Glu |
S165 |
15 | BAA10g23360 | A10 | 19691330 | G | A | upstream_gene_variant | MODIFIER | c.-298C>T| |
S193 |
16 | BAA10g23360 | A10 | 19691478 | G | A | upstream_gene_variant | MODIFIER | c.-446C>T| |
S264 |
17 | BAA10g23360 | A10 | 19694912 | G | A | upstream_gene_variant | MODIFIER | c.-3880C>T| |
S160 |
18 | BAA10g23360 | A10 | 19695978 | G | A | upstream_gene_variant | MODIFIER | c.-4946C>T| |
S57 |