Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14480 | A10 | 15168940 | G | A | missense_variant | MODERATE | c.2884C>T|p.Pro962Ser |
S293 |
2 | BAA10g14480 | A10 | 15169772 | G | A | missense_variant | MODERATE | c.2417C>T|p.Thr806Ile |
S293 |
3 | BAA10g14480 | A10 | 15170548 | C | T | missense_variant | MODERATE | c.2117G>A|p.Arg706Lys |
S301 S304 |
4 | BAA10g14480 | A10 | 15170610 | C | T | synonymous_variant | LOW | c.2055G>A|p.Arg685Arg |
S246 |
5 | BAA10g14480 | A10 | 15171464 | C | T | missense_variant | MODERATE | c.1630G>A|p.Asp544Asn |
S146 |
6 | BAA10g14480 | A10 | 15171919 | G | A | missense_variant | MODERATE | c.1358C>T|p.Ser453Phe |
S53 |
7 | BAA10g14480 | A10 | 15172306 | G | A | synonymous_variant | LOW | c.1146C>T|p.Phe382Phe |
S278 |
8 | BAA10g14480 | A10 | 15172774 | G | A | missense_variant | MODERATE | c.848C>T|p.Ser283Phe |
S179 |
9 | BAA10g14480 | A10 | 15173233 | G | A | stop_gained | HIGH | c.565C>T|p.Gln189* |
S40 S49 |
10 | BAA10g14480 | A10 | 15173463 | G | A | missense_variant | MODERATE | c.413C>T|p.Pro138Leu |
S279 |
11 | BAA10g14480 | A10 | 15173926 | G | A | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S182 |
12 | BAA10g14480 | A10 | 15178668 | C | T | upstream_gene_variant | MODIFIER | c.-4598G>A| |
S299 |