Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19570 | A10 | 17903594 | G | A | missense_variant | MODERATE | c.2365C>T|p.Pro789Ser |
S202 |
2 | BAA10g19570 | A10 | 17904177 | C | T | synonymous_variant | LOW | c.1782G>A|p.Glu594Glu |
S269 |
3 | BAA10g19570 | A10 | 17904179 | C | T | missense_variant | MODERATE | c.1780G>A|p.Glu594Lys |
S195 |
4 | BAA10g19570 | A10 | 17904819 | G | A | synonymous_variant | LOW | c.1140C>T|p.Val380Val |
S240 |
5 | BAA10g19570 | A10 | 17905990 | C | T | missense_variant | MODERATE | c.748G>A|p.Asp250Asn |
S2 |
6 | BAA10g19570 | A10 | 17906012 | C | T | synonymous_variant | LOW | c.726G>A|p.Lys242Lys |
S47 |
7 | BAA10g19570 | A10 | 17906583 | G | A | synonymous_variant | LOW | c.483C>T|p.Ser161Ser |
S118 |
8 | BAA10g19570 | A10 | 17906756 | C | T | splice_donor_variant&intron_variant | HIGH | c.414+1G>A| |
S169 |
9 | BAA10g19570 | A10 | 17907084 | G | A | splice_region_variant&intron_variant | LOW | c.235-4C>T| |
S289 S290 |
10 | BAA10g19570 | A10 | 17908339 | G | A | upstream_gene_variant | MODIFIER | c.-788C>T| |
S240 |
11 | BAA10g19570 | A10 | 17910245 | G | A | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S184 |
12 | BAA10g19570 | A10 | 17910817 | G | A | upstream_gene_variant | MODIFIER | c.-3266C>T| |
S273 |
13 | BAA10g19570 | A10 | 17910844 | G | A | upstream_gene_variant | MODIFIER | c.-3293C>T| |
S278 |
14 | BAA10g19570 | A10 | 17910894 | G | A | upstream_gene_variant | MODIFIER | c.-3343C>T| |
S228 |
15 | BAA10g19570 | A10 | 17911540 | C | T | upstream_gene_variant | MODIFIER | c.-3989G>A| |
S117 |