Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19150 | A03 | 8490278 | G | A | synonymous_variant | LOW | c.4221C>T|p.Phe1407Phe |
S95 |
2 | BAA03g19150 | A03 | 8491395 | C | T | synonymous_variant | LOW | c.3843G>A|p.Ser1281Ser |
S182 |
3 | BAA03g19150 | A03 | 8492052 | C | T | missense_variant | MODERATE | c.3535G>A|p.Val1179Ile |
S156 |
4 | BAA03g19150 | A03 | 8492504 | C | T | missense_variant | MODERATE | c.3320G>A|p.Arg1107Lys |
S131 |
5 | BAA03g19150 | A03 | 8492920 | C | T | missense_variant | MODERATE | c.3110G>A|p.Gly1037Asp |
S173 |
6 | BAA03g19150 | A03 | 8493484 | G | A | missense_variant | MODERATE | c.2908C>T|p.Arg970Cys |
S286 |
7 | BAA03g19150 | A03 | 8493520 | C | T | missense_variant | MODERATE | c.2872G>A|p.Gly958Arg |
S241 |
8 | BAA03g19150 | A03 | 8493892 | C | T | missense_variant | MODERATE | c.2662G>A|p.Glu888Lys |
S40 S49 |
9 | BAA03g19150 | A03 | 8494003 | G | A | intron_variant | MODIFIER | c.2615-64C>T| |
S76 |
10 | BAA03g19150 | A03 | 8494149 | C | T | intron_variant | MODIFIER | c.2615-210G>A| |
S45 |
11 | BAA03g19150 | A03 | 8495027 | C | T | intron_variant | MODIFIER | c.2311+16G>A| |
S58 |
12 | BAA03g19150 | A03 | 8495736 | C | T | intron_variant | MODIFIER | c.2027-71G>A| |
S15 S3 |
13 | BAA03g19150 | A03 | 8496121 | C | T | missense_variant | MODERATE | c.1933G>A|p.Val645Met |
S134 |
14 | BAA03g19150 | A03 | 8496173 | G | A | synonymous_variant | LOW | c.1881C>T|p.Pro627Pro |
S191 |
15 | BAA03g19150 | A03 | 8496447 | C | T | splice_region_variant&intron_variant | LOW | c.1730-4G>A| |
S180 |
16 | BAA03g19150 | A03 | 8497124 | C | T | missense_variant | MODERATE | c.1378G>A|p.Glu460Lys |
S117 |
17 | BAA03g19150 | A03 | 8497866 | C | T | missense_variant&splice_region_variant | MODERATE | c.1186G>A|p.Glu396Lys |
S273 |
18 | BAA03g19150 | A03 | 8498548 | G | A | synonymous_variant | LOW | c.889C>T|p.Leu297Leu |
S72 |
19 | BAA03g19150 | A03 | 8499003 | G | A | synonymous_variant | LOW | c.678C>T|p.Asp226Asp |
S249 |
20 | BAA03g19150 | A03 | 8499187 | C | T | missense_variant | MODERATE | c.494G>A|p.Arg165Lys |
S192 |
21 | BAA03g19150 | A03 | 8500216 | G | A | upstream_gene_variant | MODIFIER | c.-536C>T| |
S136 |
22 | BAA03g19150 | A03 | 8500897 | C | T | upstream_gene_variant | MODIFIER | c.-1217G>A| |
S299 |
23 | BAA03g19150 | A03 | 8501651 | C | T | upstream_gene_variant | MODIFIER | c.-1971G>A| |
S276 |
24 | BAA03g19150 | A03 | 8504517 | C | T | upstream_gene_variant | MODIFIER | c.-4837G>A| |
S223 |