Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01800 | A10 | 858844 | G | A | missense_variant | MODERATE | c.8132C>T|p.Ser2711Phe |
S168 |
2 | BAA10g01800 | A10 | 859222 | C | T | missense_variant | MODERATE | c.7754G>A|p.Arg2585His |
S244 |
3 | BAA10g01800 | A10 | 859235 | G | A | missense_variant | MODERATE | c.7741C>T|p.Leu2581Phe |
S295 |
4 | BAA10g01800 | A10 | 859619 | C | T | missense_variant | MODERATE | c.7357G>A|p.Val2453Ile |
S241 S39 |
5 | BAA10g01800 | A10 | 859632 | G | A | synonymous_variant | LOW | c.7344C>T|p.Asn2448Asn |
S64 |
6 | BAA10g01800 | A10 | 859759 | C | T | missense_variant | MODERATE | c.7217G>A|p.Cys2406Tyr |
S122 |
7 | BAA10g01800 | A10 | 860093 | C | T | missense_variant | MODERATE | c.6883G>A|p.Asp2295Asn |
S275 |
8 | BAA10g01800 | A10 | 860557 | G | A | missense_variant | MODERATE | c.6419C>T|p.Ser2140Leu |
S107 |
9 | BAA10g01800 | A10 | 861185 | C | T | intron_variant | MODIFIER | c.5817-26G>A| |
S287 |
10 | BAA10g01800 | A10 | 861345 | G | A | missense_variant | MODERATE | c.5797C>T|p.Leu1933Phe |
S219 |
11 | BAA10g01800 | A10 | 862227 | G | A | missense_variant | MODERATE | c.4915C>T|p.Pro1639Ser |
S230 |
12 | BAA10g01800 | A10 | 862853 | G | A | missense_variant | MODERATE | c.4289C>T|p.Ser1430Phe |
S76 |
13 | BAA10g01800 | A10 | 863035 | C | T | intron_variant | MODIFIER | c.4165+36G>A| |
S114 |
14 | BAA10g01800 | A10 | 863085 | G | A | missense_variant | MODERATE | c.4151C>T|p.Ala1384Val |
S251 |
15 | BAA10g01800 | A10 | 863117 | G | A | synonymous_variant | LOW | c.4119C>T|p.Leu1373Leu |
S148 S210 S30 |
16 | BAA10g01800 | A10 | 863179 | G | A | missense_variant | MODERATE | c.4057C>T|p.Leu1353Phe |
S83 S88 |
17 | BAA10g01800 | A10 | 863260 | C | T | missense_variant | MODERATE | c.3976G>A|p.Asp1326Asn |
S270 |
18 | BAA10g01800 | A10 | 863633 | G | A | synonymous_variant | LOW | c.3603C>T|p.Phe1201Phe |
S151 S263 |
19 | BAA10g01800 | A10 | 865338 | C | T | synonymous_variant | LOW | c.2232G>A|p.Thr744Thr |
S117 |
20 | BAA10g01800 | A10 | 866653 | C | T | missense_variant | MODERATE | c.1063G>A|p.Glu355Lys |
S157 |
21 | BAA10g01800 | A10 | 867720 | G | A | synonymous_variant | LOW | c.591C>T|p.Leu197Leu |
S120 |
22 | BAA10g01800 | A10 | 868976 | C | T | missense_variant | MODERATE | c.166G>A|p.Asp56Asn |
S60 |
23 | BAA10g01800 | A10 | 868997 | C | T | missense_variant | MODERATE | c.145G>A|p.Ala49Thr |
S23 |
24 | BAA10g01800 | A10 | 869574 | C | T | upstream_gene_variant | MODIFIER | c.-433G>A| |
S67 |
25 | BAA10g01800 | A10 | 870064 | C | T | upstream_gene_variant | MODIFIER | c.-923G>A| |
S31 |