Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g42230 | A06 | 27437944 | C | T | upstream_gene_variant | MODIFIER | c.-2435C>T| |
S252 |
2 | BAA06g42230 | A06 | 27439149 | C | T | upstream_gene_variant | MODIFIER | c.-1230C>T| |
S97 |
3 | BAA06g42230 | A06 | 27440550 | G | A | synonymous_variant | LOW | c.93G>A|p.Gln31Gln |
S199 |
4 | BAA06g42230 | A06 | 27442231 | C | T | missense_variant | MODERATE | c.1159C>T|p.Leu387Phe |
S15 S3 |
5 | BAA06g42230 | A06 | 27443129 | G | A | splice_region_variant&intron_variant | LOW | c.1647+7G>A| |
S289 S290 |
6 | BAA06g42230 | A06 | 27443414 | G | A | missense_variant | MODERATE | c.1798G>A|p.Gly600Ser |
S23 |
7 | BAA06g42230 | A06 | 27443779 | C | T | splice_region_variant&intron_variant | LOW | c.2017-3C>T| |
S282 |
8 | BAA06g42230 | A06 | 27443885 | C | T | missense_variant | MODERATE | c.2120C>T|p.Thr707Ile |
S165 |
9 | BAA06g42230 | A06 | 27444871 | C | T | missense_variant | MODERATE | c.2849C>T|p.Ser950Phe |
S112 |
10 | BAA06g42230 | A06 | 27445017 | G | A | downstream_gene_variant | MODIFIER | c.*70G>A| |
S268 |
11 | BAA06g42230 | A06 | 27445551 | C | T | downstream_gene_variant | MODIFIER | c.*604C>T| |
S235 |
12 | BAA06g42230 | A06 | 27446415 | C | T | downstream_gene_variant | MODIFIER | c.*1468C>T| |
S134 S48 |