Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26290 | A10 | 20909251 | C | T | splice_region_variant&intron_variant | LOW | c.630+7C>T| |
S153 S213 |
2 | BAA10g26290 | A10 | 20909386 | G | A | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S164 |
3 | BAA10g26290 | A10 | 20911385 | G | A | synonymous_variant | LOW | c.1572G>A|p.Leu524Leu |
S67 |
4 | BAA10g26290 | A10 | 20913025 | C | T | intron_variant | MODIFIER | c.2513+15C>T| |
S133 |
5 | BAA10g26290 | A10 | 20913283 | G | A | missense_variant | MODERATE | c.2645G>A|p.Arg882Lys |
S67 |
6 | BAA10g26290 | A10 | 20914794 | C | T | missense_variant | MODERATE | c.3476C>T|p.Ala1159Val |
S155 S211 |
7 | BAA10g26290 | A10 | 20914936 | C | T | synonymous_variant | LOW | c.3546C>T|p.Leu1182Leu |
S206 S26 |
8 | BAA10g26290 | A10 | 20916634 | C | T | splice_region_variant&intron_variant | LOW | c.4584+4C>T| |
S168 |
9 | BAA10g26290 | A10 | 20916893 | G | A | missense_variant | MODERATE | c.4769G>A|p.Gly1590Glu |
S63 |
10 | BAA10g26290 | A10 | 20917453 | C | T | stop_gained | HIGH | c.5329C>T|p.Gln1777* |
S8 |
11 | BAA10g26290 | A10 | 20917491 | G | A | synonymous_variant | LOW | c.5367G>A|p.Arg1789Arg |
S256 |
12 | BAA10g26290 | A10 | 20922495 | G | T | downstream_gene_variant | MODIFIER | c.*4251G>T| |
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