Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00570 | A08 | 388707 | G | A | missense_variant | MODERATE | c.214G>A|p.Asp72Asn |
S206 |
2 | BAA08g00570 | A08 | 388792 | G | A | missense_variant | MODERATE | c.299G>A|p.Gly100Glu |
S94 |
3 | BAA08g00570 | A08 | 389923 | C | T | intron_variant | MODIFIER | c.715+139C>T| |
S8 |
4 | BAA08g00570 | A08 | 391053 | G | A | intron_variant | MODIFIER | c.1091-35G>A| |
S192 |
5 | BAA08g00570 | A08 | 392114 | C | T | synonymous_variant | LOW | c.2032C>T|p.Leu678Leu |
S148 S210 S30 S31 |
6 | BAA08g00570 | A08 | 392422 | C | T | intron_variant | MODIFIER | c.2221-47C>T| |
S172 S217 |
7 | BAA08g00570 | A08 | 392577 | G | A | missense_variant | MODERATE | c.2329G>A|p.Glu777Lys |
S40 S49 |
8 | BAA08g00570 | A08 | 393845 | C | T | missense_variant | MODERATE | c.2713C>T|p.Leu905Phe |
S7 |
9 | BAA08g00570 | A08 | 394268 | G | A | splice_region_variant&intron_variant | LOW | c.3034-4G>A| |
S95 |
10 | BAA08g00570 | A08 | 394720 | C | T | missense_variant | MODERATE | c.3380C>T|p.Ser1127Phe |
S308 |
11 | BAA08g00570 | A08 | 394923 | C | T | missense_variant | MODERATE | c.3583C>T|p.Pro1195Ser |
S153 S213 |
12 | BAA08g00570 | A08 | 395615 | G | A | missense_variant | MODERATE | c.4180G>A|p.Glu1394Lys |
S194 |
13 | BAA08g00570 | A08 | 395972 | G | A | missense_variant | MODERATE | c.4537G>A|p.Glu1513Lys |
S188 |