Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g19560 | A07 | 25212965 | C | T | missense_variant | MODERATE | c.7646G>A|p.Arg2549Lys |
S5 |
2 | BAA07g19560 | A07 | 25212970 | C | T | synonymous_variant | LOW | c.7641G>A|p.Gln2547Gln |
S232 |
3 | BAA07g19560 | A07 | 25212990 | C | T | missense_variant | MODERATE | c.7621G>A|p.Asp2541Asn |
S143 |
4 | BAA07g19560 | A07 | 25213103 | G | A | missense_variant | MODERATE | c.7609C>T|p.Pro2537Ser |
S104 |
5 | BAA07g19560 | A07 | 25213500 | G | A | intron_variant | MODIFIER | c.7371+41C>T| |
S264 |
6 | BAA07g19560 | A07 | 25214575 | C | T | synonymous_variant | LOW | c.6534G>A|p.Lys2178Lys |
S283 |
7 | BAA07g19560 | A07 | 25216693 | T | C | synonymous_variant | LOW | c.4416A>G|p.Lys1472Lys |
S121 |
8 | BAA07g19560 | A07 | 25216844 | G | A | missense_variant | MODERATE | c.4265C>T|p.Pro1422Leu |
S186 |
9 | BAA07g19560 | A07 | 25220474 | C | T | missense_variant | MODERATE | c.1324G>A|p.Glu442Lys |
S150 |
10 | BAA07g19560 | A07 | 25223925 | G | A | upstream_gene_variant | MODIFIER | c.-1163C>T| |
S6 |
11 | BAA07g19560 | A07 | 25224438 | G | A | upstream_gene_variant | MODIFIER | c.-1676C>T| |
S301 |
12 | BAA07g19560 | A07 | 25225655 | G | A | upstream_gene_variant | MODIFIER | c.-2893C>T| |
S107 |
13 | BAA07g19560 | A07 | 25227692 | G | A | upstream_gene_variant | MODIFIER | c.-4930C>T| |
S296 |