Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45030 | A09 | 50365260 | G | A | missense_variant&splice_region_variant | MODERATE | c.1324G>A|p.Asp442Asn |
S45 |
2 | BAA09g45030 | A09 | 50365740 | G | A | missense_variant | MODERATE | c.1591G>A|p.Ala531Thr |
S12 |
3 | BAA09g45030 | A09 | 50365839 | G | A | missense_variant | MODERATE | c.1690G>A|p.Glu564Lys |
S140 S168 S219 S64 S72 |
4 | BAA09g45030 | A09 | 50365929 | C | T | missense_variant | MODERATE | c.1780C>T|p.Pro594Ser |
S228 |
5 | BAA09g45030 | A09 | 50366001 | C | T | synonymous_variant | LOW | c.1852C>T|p.Leu618Leu |
S63 |
6 | BAA09g45030 | A09 | 50366317 | G | A | missense_variant | MODERATE | c.2168G>A|p.Arg723Lys |
S34 |
7 | BAA09g45030 | A09 | 50367144 | C | T | missense_variant | MODERATE | c.2456C>T|p.Pro819Leu |
S208 S89 |
8 | BAA09g45030 | A09 | 50367385 | G | A | synonymous_variant | LOW | c.2697G>A|p.Lys899Lys |
S288 |
9 | BAA09g45030 | A09 | 50368059 | C | T | missense_variant | MODERATE | c.3371C>T|p.Ser1124Phe |
S206 S26 |
10 | BAA09g45030 | A09 | 50368121 | G | A | missense_variant | MODERATE | c.3433G>A|p.Glu1145Lys |
S200 |
11 | BAA09g45030 | A09 | 50368261 | C | T | synonymous_variant | LOW | c.3573C>T|p.Ala1191Ala |
S18 |
12 | BAA09g45030 | A09 | 50368313 | G | A | missense_variant | MODERATE | c.3625G>A|p.Asp1209Asn |
S246 |
13 | BAA09g45030 | A09 | 50368686 | G | A | missense_variant | MODERATE | c.3998G>A|p.Arg1333Lys |
S166 |
14 | BAA09g45030 | A09 | 50368966 | G | A | synonymous_variant | LOW | c.4278G>A|p.Thr1426Thr |
S249 |
15 | BAA09g45030 | A09 | 50369280 | C | T | missense_variant | MODERATE | c.4592C>T|p.Pro1531Leu |
S279 |
16 | BAA09g45030 | A09 | 50369344 | G | A | synonymous_variant | LOW | c.4656G>A|p.Gln1552Gln |
S281 |