Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g27860 | A07 | 29392788 | C | T | missense_variant | MODERATE | c.2836G>A|p.Glu946Lys |
S136 |
2 | BAA07g27860 | A07 | 29394439 | G | A | missense_variant | MODERATE | c.2224C>T|p.Arg742Cys |
S139 |
3 | BAA07g27860 | A07 | 29396871 | G | A | synonymous_variant | LOW | c.1359C>T|p.Pro453Pro |
S138 |
4 | BAA07g27860 | A07 | 29397078 | G | A | intron_variant | MODIFIER | c.1299+105C>T| |
S50 |
5 | BAA07g27860 | A07 | 29397264 | C | T | synonymous_variant | LOW | c.1218G>A|p.Arg406Arg |
S71 |
6 | BAA07g27860 | A07 | 29398377 | C | T | synonymous_variant | LOW | c.732G>A|p.Lys244Lys |
S174 S27 |
7 | BAA07g27860 | A07 | 29399472 | C | T | missense_variant&splice_region_variant | MODERATE | c.238G>A|p.Glu80Lys |
S196 |
8 | BAA07g27860 | A07 | 29399722 | G | A | synonymous_variant | LOW | c.234C>T|p.Leu78Leu |
S38 |
9 | BAA07g27860 | A07 | 29399762 | G | A | missense_variant | MODERATE | c.194C>T|p.Ser65Phe |
S272 |
10 | BAA07g27860 | A07 | 29399780 | C | T | missense_variant | MODERATE | c.176G>A|p.Gly59Asp |
S17 |
11 | BAA07g27860 | A07 | 29400141 | G | A | upstream_gene_variant | MODIFIER | c.-186C>T| |
S219 |
12 | BAA07g27860 | A07 | 29400585 | G | A | upstream_gene_variant | MODIFIER | c.-630C>T| |
S35 |
13 | BAA07g27860 | A07 | 29400998 | C | T | upstream_gene_variant | MODIFIER | c.-1043G>A| |
S197 |
14 | BAA07g27860 | A07 | 29401194 | C | T | upstream_gene_variant | MODIFIER | c.-1239G>A| |
S216 |
15 | BAA07g27860 | A07 | 29401868 | G | A | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S1 S90 |
16 | BAA07g27860 | A07 | 29402894 | G | A | upstream_gene_variant | MODIFIER | c.-2939C>T| |
S69 |
17 | BAA07g27860 | A07 | 29403146 | G | A | upstream_gene_variant | MODIFIER | c.-3191C>T| |
S53 |
18 | BAA07g27860 | A07 | 29403771 | C | T | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S81 S85 |
19 | BAA07g27860 | A07 | 29404752 | G | A | upstream_gene_variant | MODIFIER | c.-4797C>T| |
S271 |
20 | BAA07g27860 | A07 | 29404759 | C | T | upstream_gene_variant | MODIFIER | c.-4804G>A| |
S270 |
21 | BAA07g27860 | A07 | 29404923 | G | A | upstream_gene_variant | MODIFIER | c.-4968C>T| |
S171 |