Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22410 | A10 | 19263941 | C | T | downstream_gene_variant | MODIFIER | c.*1654G>A| |
S46 |
2 | BAA10g22410 | A10 | 19265024 | C | T | downstream_gene_variant | MODIFIER | c.*571G>A| |
S76 |
3 | BAA10g22410 | A10 | 19265066 | T | A | downstream_gene_variant | MODIFIER | c.*529A>T| |
S202 |
4 | BAA10g22410 | A10 | 19266625 | C | T | splice_region_variant&intron_variant | LOW | c.2287+8G>A| |
S10 |
5 | BAA10g22410 | A10 | 19267241 | C | T | missense_variant | MODERATE | c.1765G>A|p.Asp589Asn |
S197 |
6 | BAA10g22410 | A10 | 19267588 | C | T | missense_variant | MODERATE | c.1504G>A|p.Glu502Lys |
S130 |
7 | BAA10g22410 | A10 | 19268050 | G | A | missense_variant | MODERATE | c.1241C>T|p.Thr414Ile |
S172 S217 |
8 | BAA10g22410 | A10 | 19268479 | G | A | synonymous_variant | LOW | c.1002C>T|p.Ala334Ala |
S16 |
9 | BAA10g22410 | A10 | 19269006 | G | A | missense_variant | MODERATE | c.599C>T|p.Ala200Val |
S9 |
10 | BAA10g22410 | A10 | 19270928 | C | T | upstream_gene_variant | MODIFIER | c.-856G>A| |
S8 |
11 | BAA10g22410 | A10 | 19272163 | C | T | upstream_gene_variant | MODIFIER | c.-2091G>A| |
S135 |
12 | BAA10g22410 | A10 | 19273258 | G | A | upstream_gene_variant | MODIFIER | c.-3186C>T| |
S218 |