Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16140 | A10 | 16112037 | C | T | upstream_gene_variant | MODIFIER | c.-64C>T| |
S45 |
2 | BAA10g16140 | A10 | 16112581 | C | T | missense_variant | MODERATE | c.247C>T|p.Leu83Phe |
S5 |
3 | BAA10g16140 | A10 | 16112759 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.316-1G>A| |
S262 |
4 | BAA10g16140 | A10 | 16112812 | C | T | missense_variant | MODERATE | c.368C>T|p.Ser123Phe |
S10 |
5 | BAA10g16140 | A10 | 16113540 | G | A | missense_variant | MODERATE | c.583G>A|p.Glu195Lys |
S1 |
6 | BAA10g16140 | A10 | 16115208 | G | A | missense_variant | MODERATE | c.2059G>A|p.Gly687Arg |
S219 |
7 | BAA10g16140 | A10 | 16115658 | C | T | missense_variant | MODERATE | c.2341C>T|p.Leu781Phe |
S237 |
8 | BAA10g16140 | A10 | 16116189 | G | A | missense_variant | MODERATE | c.2872G>A|p.Glu958Lys |
S262 |
9 | BAA10g16140 | A10 | 16116949 | G | A | missense_variant | MODERATE | c.3632G>A|p.Ser1211Asn |
S198 |
10 | BAA10g16140 | A10 | 16117316 | C | T | missense_variant | MODERATE | c.3782C>T|p.Pro1261Leu |
S53 |
11 | BAA10g16140 | A10 | 16118356 | G | A | missense_variant | MODERATE | c.4736G>A|p.Gly1579Glu |
S289 |
12 | BAA10g16140 | A10 | 16118704 | G | A | missense_variant | MODERATE | c.5084G>A|p.Arg1695Lys |
S67 |
13 | BAA10g16140 | A10 | 16118843 | C | T | splice_region_variant&intron_variant | LOW | c.5128-3C>T| |
S281 |
14 | BAA10g16140 | A10 | 16119235 | C | T | synonymous_variant | LOW | c.5400C>T|p.Asn1800Asn |
S162 |
15 | BAA10g16140 | A10 | 16119367 | G | A | synonymous_variant | LOW | c.5532G>A|p.Lys1844Lys |
S198 |