Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41690 | A05 | 39724923 | C | T | missense_variant | MODERATE | c.4088G>A|p.Arg1363Lys |
S128 |
2 | BAA05g41690 | A05 | 39725871 | G | A | missense_variant | MODERATE | c.3293C>T|p.Ala1098Val |
S80 |
3 | BAA05g41690 | A05 | 39726453 | C | T | synonymous_variant | LOW | c.2886G>A|p.Lys962Lys |
S97 |
4 | BAA05g41690 | A05 | 39726528 | C | T | missense_variant | MODERATE | c.2811G>A|p.Met937Ile |
S250 |
5 | BAA05g41690 | A05 | 39727156 | G | A | missense_variant | MODERATE | c.2338C>T|p.Pro780Ser |
S47 |
6 | BAA05g41690 | A05 | 39727366 | C | T | splice_donor_variant&intron_variant | HIGH | c.2208+1G>A| |
S54 |
7 | BAA05g41690 | A05 | 39727766 | C | T | missense_variant | MODERATE | c.1885G>A|p.Asp629Asn |
S282 |
8 | BAA05g41690 | A05 | 39729616 | G | A | missense_variant | MODERATE | c.683C>T|p.Pro228Leu |
S51 |
9 | BAA05g41690 | A05 | 39729937 | C | T | missense_variant | MODERATE | c.532G>A|p.Val178Ile |
S41 |
10 | BAA05g41690 | A05 | 39730525 | G | A | stop_gained | HIGH | c.337C>T|p.Gln113* |
S262 |
11 | BAA05g41690 | A05 | 39730965 | G | A | missense_variant | MODERATE | c.160C>T|p.Leu54Phe |
S36 |
12 | BAA05g41690 | A05 | 39731401 | C | T | upstream_gene_variant | MODIFIER | c.-201G>A| |
S162 |
13 | BAA05g41690 | A05 | 39731979 | G | A | upstream_gene_variant | MODIFIER | c.-779C>T| |
S1 S90 |
14 | BAA05g41690 | A05 | 39734152 | G | A | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S19 |