Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18750 | A09 | 11276785 | G | A | downstream_gene_variant | MODIFIER | c.*507C>T| |
S245 |
2 | BAA09g18750 | A09 | 11277049 | G | A | downstream_gene_variant | MODIFIER | c.*243C>T| |
S146 |
3 | BAA09g18750 | A09 | 11277981 | G | A | intron_variant | MODIFIER | c.4115-670C>T| |
S121 |
4 | BAA09g18750 | A09 | 11278050 | G | A | intron_variant | MODIFIER | c.4115-739C>T| |
S130 |
5 | BAA09g18750 | A09 | 11278164 | G | A | intron_variant | MODIFIER | c.4115-853C>T| |
S162 |
6 | BAA09g18750 | A09 | 11281159 | G | A | intron_variant | MODIFIER | c.4114+2224C>T| |
S204 |
7 | BAA09g18750 | A09 | 11282968 | C | T | intron_variant | MODIFIER | c.4114+415G>A| |
S50 |
8 | BAA09g18750 | A09 | 11284041 | G | A | synonymous_variant | LOW | c.3525C>T|p.Ile1175Ile |
S122 |
9 | BAA09g18750 | A09 | 11284568 | T | A | missense_variant | MODERATE | c.3234A>T|p.Gln1078His |
S126 |
10 | BAA09g18750 | A09 | 11285599 | C | T | missense_variant | MODERATE | c.3032G>A|p.Arg1011Lys |
S5 |
11 | BAA09g18750 | A09 | 11285866 | C | T | missense_variant | MODERATE | c.2765G>A|p.Arg922Lys |
S182 |
12 | BAA09g18750 | A09 | 11286256 | G | A | intron_variant | MODIFIER | c.2531-58C>T| |
S149 |
13 | BAA09g18750 | A09 | 11286614 | C | T | splice_region_variant&synonymous_variant | LOW | c.2376G>A|p.Lys792Lys |
S35 |
14 | BAA09g18750 | A09 | 11286670 | G | T | missense_variant | MODERATE | c.2320C>A|p.Gln774Lys |
S298 |
15 | BAA09g18750 | A09 | 11287393 | G | A | synonymous_variant | LOW | c.1834C>T|p.Leu612Leu |
S185 |
16 | BAA09g18750 | A09 | 11287482 | G | A | missense_variant | MODERATE | c.1745C>T|p.Ser582Phe |
S38 |
17 | BAA09g18750 | A09 | 11287764 | G | A | missense_variant | MODERATE | c.1463C>T|p.Thr488Ile |
S47 |
18 | BAA09g18750 | A09 | 11287874 | G | A | synonymous_variant | LOW | c.1353C>T|p.Gly451Gly |
S245 |
19 | BAA09g18750 | A09 | 11287924 | G | A | missense_variant | MODERATE | c.1303C>T|p.Pro435Ser |
S80 |
20 | BAA09g18750 | A09 | 11288210 | C | T | missense_variant | MODERATE | c.1102G>A|p.Asp368Asn |
S64 |
21 | BAA09g18750 | A09 | 11288530 | C | T | missense_variant | MODERATE | c.893G>A|p.Gly298Glu |
S36 |
22 | BAA09g18750 | A09 | 11288652 | G | A | synonymous_variant | LOW | c.771C>T|p.Ala257Ala |
S276 |
23 | BAA09g18750 | A09 | 11289142 | G | A | missense_variant | MODERATE | c.455C>T|p.Pro152Leu |
S245 |
24 | BAA09g18750 | A09 | 11289198 | C | T | synonymous_variant | LOW | c.399G>A|p.Gln133Gln |
S50 |
25 | BAA09g18750 | A09 | 11289339 | G | A | synonymous_variant | LOW | c.258C>T|p.Thr86Thr |
S189 |