Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06810 | A01 | 3017275 | G | A | missense_variant | MODERATE | c.5272C>T|p.Pro1758Ser |
S115 |
2 | BAA01g06810 | A01 | 3017508 | C | T | missense_variant | MODERATE | c.5137G>A|p.Ala1713Thr |
S135 |
3 | BAA01g06810 | A01 | 3017692 | C | T | stop_gained | HIGH | c.4953G>A|p.Trp1651* |
S265 |
4 | BAA01g06810 | A01 | 3018312 | G | A | missense_variant | MODERATE | c.4409C>T|p.Ala1470Val |
S292 |
5 | BAA01g06810 | A01 | 3018332 | C | T | synonymous_variant | LOW | c.4389G>A|p.Gln1463Gln |
S81 S85 |
6 | BAA01g06810 | A01 | 3018436 | C | T | missense_variant | MODERATE | c.4285G>A|p.Glu1429Lys |
S16 |
7 | BAA01g06810 | A01 | 3018917 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3805-1G>A| |
S132 S137 S215 |
8 | BAA01g06810 | A01 | 3019461 | C | T | missense_variant | MODERATE | c.3359G>A|p.Ser1120Asn |
S99 |
9 | BAA01g06810 | A01 | 3020045 | G | A | synonymous_variant | LOW | c.2775C>T|p.Asp925Asp |
S197 |
10 | BAA01g06810 | A01 | 3020827 | C | T | missense_variant | MODERATE | c.1993G>A|p.Glu665Lys |
S51 |
11 | BAA01g06810 | A01 | 3020919 | G | A | missense_variant | MODERATE | c.1901C>T|p.Ser634Phe |
S221 |
12 | BAA01g06810 | A01 | 3021388 | C | T | missense_variant | MODERATE | c.1432G>A|p.Glu478Lys |
S18 |
13 | BAA01g06810 | A01 | 3021559 | C | T | missense_variant | MODERATE | c.1261G>A|p.Ala421Thr |
S139 |
14 | BAA01g06810 | A01 | 3022009 | G | A | missense_variant | MODERATE | c.811C>T|p.Pro271Ser |
S6 |
15 | BAA01g06810 | A01 | 3022429 | C | T | missense_variant | MODERATE | c.391G>A|p.Asp131Asn |
S104 S52 |
16 | BAA01g06810 | A01 | 3025055 | G | T | upstream_gene_variant | MODIFIER | c.-2036C>A| |
S280 |
17 | BAA01g06810 | A01 | 3025917 | C | T | upstream_gene_variant | MODIFIER | c.-2898G>A| |
S246 |
18 | BAA01g06810 | A01 | 3027247 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S297 |