Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03040 | A10 | 1484225 | C | T | missense_variant | MODERATE | c.2518G>A|p.Gly840Arg |
S54 |
2 | BAA10g03040 | A10 | 1484232 | G | A | synonymous_variant | LOW | c.2511C>T|p.Phe837Phe |
S178 |
3 | BAA10g03040 | A10 | 1484308 | C | T | missense_variant | MODERATE | c.2435G>A|p.Cys812Tyr |
S247 |
4 | BAA10g03040 | A10 | 1484686 | G | A | missense_variant | MODERATE | c.2126C>T|p.Ser709Phe |
S276 |
5 | BAA10g03040 | A10 | 1485210 | C | T | synonymous_variant | LOW | c.1602G>A|p.Gln534Gln |
S256 |
6 | BAA10g03040 | A10 | 1485667 | G | A | missense_variant | MODERATE | c.1214C>T|p.Ser405Phe |
S219 S72 |
7 | BAA10g03040 | A10 | 1487190 | C | T | start_lost | HIGH | c.3G>A|p.Met1? |
S298 |
8 | BAA10g03040 | A10 | 1488284 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S13 |
9 | BAA10g03040 | A10 | 1488442 | C | T | upstream_gene_variant | MODIFIER | c.-1250G>A| |
S199 |
10 | BAA10g03040 | A10 | 1488445 | G | A | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S279 |
11 | BAA10g03040 | A10 | 1488896 | G | A | upstream_gene_variant | MODIFIER | c.-1704C>T| |
S25 |
12 | BAA10g03040 | A10 | 1489029 | G | A | upstream_gene_variant | MODIFIER | c.-1837C>T| |
S243 |
13 | BAA10g03040 | A10 | 1489276 | G | A | upstream_gene_variant | MODIFIER | c.-2084C>T| |
S18 |
14 | BAA10g03040 | A10 | 1489533 | G | A | upstream_gene_variant | MODIFIER | c.-2341C>T| |
S112 |
15 | BAA10g03040 | A10 | 1490586 | A | G | upstream_gene_variant | MODIFIER | c.-3394T>C| |
S47 |
16 | BAA10g03040 | A10 | 1491942 | G | A | upstream_gene_variant | MODIFIER | c.-4750C>T| |
S148 S30 |