Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g30220 | A10 | 22491616 | G | A | missense_variant | MODERATE | c.32G>A|p.Gly11Glu |
S171 |
2 | BAA10g30220 | A10 | 22491897 | C | T | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S25 |
3 | BAA10g30220 | A10 | 22492077 | G | A | missense_variant | MODERATE | c.307G>A|p.Glu103Lys |
S270 |
4 | BAA10g30220 | A10 | 22492162 | G | A | missense_variant | MODERATE | c.392G>A|p.Gly131Glu |
S122 |
5 | BAA10g30220 | A10 | 22493111 | G | A | missense_variant | MODERATE | c.1021G>A|p.Gly341Arg |
S151 S167 S236 S257 S262 S263 |
6 | BAA10g30220 | A10 | 22493137 | C | T | synonymous_variant | LOW | c.1047C>T|p.Tyr349Tyr |
S10 |
7 | BAA10g30220 | A10 | 22493491 | G | A | missense_variant | MODERATE | c.1163G>A|p.Gly388Glu |
S197 |
8 | BAA10g30220 | A10 | 22493567 | C | T | synonymous_variant | LOW | c.1239C>T|p.Ser413Ser |
S155 S211 |
9 | BAA10g30220 | A10 | 22493639 | C | T | synonymous_variant | LOW | c.1311C>T|p.Ser437Ser |
S105 |
10 | BAA10g30220 | A10 | 22494490 | G | A | missense_variant | MODERATE | c.1860G>A|p.Met620Ile |
S263 |
11 | BAA10g30220 | A10 | 22495361 | G | A | missense_variant | MODERATE | c.2483G>A|p.Arg828Lys |
S54 |