Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11270 | A06 | 5721622 | G | A | missense_variant | MODERATE | c.2980C>T|p.Pro994Ser |
S284 |
2 | BAA06g11270 | A06 | 5722496 | C | T | missense_variant | MODERATE | c.2260G>A|p.Glu754Lys |
S280 |
3 | BAA06g11270 | A06 | 5723442 | C | T | missense_variant | MODERATE | c.1665G>A|p.Met555Ile |
S225 S73 |
4 | BAA06g11270 | A06 | 5723494 | G | A | missense_variant | MODERATE | c.1613C>T|p.Ala538Val |
S251 |
5 | BAA06g11270 | A06 | 5723985 | C | T | synonymous_variant | LOW | c.1122G>A|p.Lys374Lys |
S175 |
6 | BAA06g11270 | A06 | 5724470 | C | T | missense_variant | MODERATE | c.637G>A|p.Asp213Asn |
S120 |
7 | BAA06g11270 | A06 | 5724777 | C | T | synonymous_variant | LOW | c.330G>A|p.Arg110Arg |
S135 |
8 | BAA06g11270 | A06 | 5724875 | C | T | missense_variant | MODERATE | c.232G>A|p.Gly78Ser |
S78 |
9 | BAA06g11270 | A06 | 5725418 | C | T | upstream_gene_variant | MODIFIER | c.-312G>A| |
S65 |
10 | BAA06g11270 | A06 | 5726127 | C | T | upstream_gene_variant | MODIFIER | c.-1021G>A| |
S89 |
11 | BAA06g11270 | A06 | 5726430 | G | A | upstream_gene_variant | MODIFIER | c.-1324C>T| |
S203 |
12 | BAA06g11270 | A06 | 5727297 | C | T | upstream_gene_variant | MODIFIER | c.-2191G>A| |
S279 |
13 | BAA06g11270 | A06 | 5727437 | C | T | upstream_gene_variant | MODIFIER | c.-2331G>A| |
S301 S304 |
14 | BAA06g11270 | A06 | 5727725 | G | A | upstream_gene_variant | MODIFIER | c.-2619C>T| |
S37 |
15 | BAA06g11270 | A06 | 5727858 | G | A | upstream_gene_variant | MODIFIER | c.-2752C>T| |
S165 |
16 | BAA06g11270 | A06 | 5728384 | C | T | upstream_gene_variant | MODIFIER | c.-3278G>A| |
S270 |
17 | BAA06g11270 | A06 | 5729636 | C | T | upstream_gene_variant | MODIFIER | c.-4530G>A| |
S245 |
18 | BAA06g11270 | A06 | 5729672 | C | T | upstream_gene_variant | MODIFIER | c.-4566G>A| |
S270 |