Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g31800 | A09 | 40208763 | C | T | downstream_gene_variant | MODIFIER | c.*4661G>A| |
S117 |
2 | BAA09g31800 | A09 | 40209188 | G | A | downstream_gene_variant | MODIFIER | c.*4236C>T| |
S298 |
3 | BAA09g31800 | A09 | 40209470 | G | A | downstream_gene_variant | MODIFIER | c.*3954C>T| |
S17 |
4 | BAA09g31800 | A09 | 40214243 | G | A | missense_variant | MODERATE | c.938C>T|p.Ser313Leu |
S13 |
5 | BAA09g31800 | A09 | 40214384 | G | A | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S280 |
6 | BAA09g31800 | A09 | 40214609 | G | A | intron_variant | MODIFIER | c.685-113C>T| |
S87 |
7 | BAA09g31800 | A09 | 40215764 | G | A | intron_variant | MODIFIER | c.684+49C>T| |
S39 |
8 | BAA09g31800 | A09 | 40215812 | C | T | splice_donor_variant&intron_variant | HIGH | c.684+1G>A| |
S182 |
9 | BAA09g31800 | A09 | 40216140 | G | A | synonymous_variant | LOW | c.357C>T|p.Leu119Leu |
S196 |
10 | BAA09g31800 | A09 | 40216174 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Phe |
S281 |
11 | BAA09g31800 | A09 | 40216892 | C | T | intron_variant | MODIFIER | c.164+442G>A| |
S104 S52 |
12 | BAA09g31800 | A09 | 40217005 | C | T | intron_variant | MODIFIER | c.164+329G>A| |
S292 |
13 | BAA09g31800 | A09 | 40217331 | C | T | splice_region_variant&intron_variant | LOW | c.164+3G>A| |
S257 |
14 | BAA09g31800 | A09 | 40217685 | G | A | upstream_gene_variant | MODIFIER | c.-96C>T| |
S12 |