Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22420 | A10 | 19273670 | G | A | missense_variant | MODERATE | c.4292C>T|p.Thr1431Ile |
S228 |
2 | BAA10g22420 | A10 | 19274690 | C | T | missense_variant | MODERATE | c.3272G>A|p.Arg1091Gln |
S226 |
3 | BAA10g22420 | A10 | 19275343 | C | T | missense_variant | MODERATE | c.2887G>A|p.Glu963Lys |
S165 |
4 | BAA10g22420 | A10 | 19276882 | G | A | missense_variant | MODERATE | c.1348C>T|p.Pro450Ser |
S35 |
5 | BAA10g22420 | A10 | 19276916 | C | T | synonymous_variant | LOW | c.1314G>A|p.Glu438Glu |
S19 |
6 | BAA10g22420 | A10 | 19276951 | G | A | missense_variant | MODERATE | c.1279C>T|p.Pro427Ser |
S276 |
7 | BAA10g22420 | A10 | 19276970 | G | A | synonymous_variant | LOW | c.1260C>T|p.Phe420Phe |
S239 |
8 | BAA10g22420 | A10 | 19277117 | C | T | synonymous_variant | LOW | c.1113G>A|p.Arg371Arg |
S244 |
9 | BAA10g22420 | A10 | 19277313 | G | A | missense_variant | MODERATE | c.917C>T|p.Pro306Leu |
S59 |
10 | BAA10g22420 | A10 | 19277968 | C | T | missense_variant | MODERATE | c.262G>A|p.Glu88Lys |
S11 |
11 | BAA10g22420 | A10 | 19278152 | C | T | stop_gained | HIGH | c.78G>A|p.Trp26* |
S18 |
12 | BAA10g22420 | A10 | 19278244 | C | T | upstream_gene_variant | MODIFIER | c.-15G>A| |
S162 |
13 | BAA10g22420 | A10 | 19279108 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S211 |
14 | BAA10g22420 | A10 | 19281241 | G | A | upstream_gene_variant | MODIFIER | c.-3012C>T| |
S173 |
15 | BAA10g22420 | A10 | 19281783 | G | A | upstream_gene_variant | MODIFIER | c.-3554C>T| |
S192 |
16 | BAA10g22420 | A10 | 19281889 | C | T | upstream_gene_variant | MODIFIER | c.-3660G>A| |
S148 S210 S30 S31 |
17 | BAA10g22420 | A10 | 19282073 | G | A | upstream_gene_variant | MODIFIER | c.-3844C>T| |
S103 |