Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19420 | A08 | 15281129 | C | T | synonymous_variant | LOW | c.243C>T|p.Leu81Leu |
S208 S219 |
2 | BAA08g19420 | A08 | 15281695 | C | T | missense_variant | MODERATE | c.634C>T|p.Pro212Ser |
S291 |
3 | BAA08g19420 | A08 | 15282561 | G | A | missense_variant | MODERATE | c.1237G>A|p.Asp413Asn |
S35 |
4 | BAA08g19420 | A08 | 15283205 | C | T | missense_variant | MODERATE | c.1682C>T|p.Thr561Ile |
S134 |
5 | BAA08g19420 | A08 | 15283398 | C | T | synonymous_variant | LOW | c.1875C>T|p.Gly625Gly |
S178 |
6 | BAA08g19420 | A08 | 15283447 | G | A | missense_variant | MODERATE | c.1924G>A|p.Glu642Lys |
S282 |
7 | BAA08g19420 | A08 | 15284126 | C | T | missense_variant | MODERATE | c.2291C>T|p.Ala764Val |
S6 |
8 | BAA08g19420 | A08 | 15284710 | C | T | missense_variant | MODERATE | c.2705C>T|p.Thr902Ile |
S143 |
9 | BAA08g19420 | A08 | 15285411 | C | T | stop_gained | HIGH | c.2926C>T|p.Gln976* |
S171 |
10 | BAA08g19420 | A08 | 15286138 | G | A | missense_variant&splice_region_variant | MODERATE | c.3265G>A|p.Asp1089Asn |
S86 |
11 | BAA08g19420 | A08 | 15286888 | G | A | missense_variant | MODERATE | c.3734G>A|p.Arg1245Lys |
S90 |
12 | BAA08g19420 | A08 | 15287370 | G | A | missense_variant | MODERATE | c.4216G>A|p.Glu1406Lys |
S181 |
13 | BAA08g19420 | A08 | 15287986 | C | T | missense_variant | MODERATE | c.4832C>T|p.Pro1611Leu |
S250 S76 |
14 | BAA08g19420 | A08 | 15288076 | C | T | missense_variant | MODERATE | c.4922C>T|p.Ser1641Phe |
S215 |