Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00020 | A06 | 36021 | C | A | missense_variant | MODERATE | c.3475G>T|p.Val1159Phe |
S79 |
2 | BAA06g00020 | A06 | 36170 | G | A | synonymous_variant | LOW | c.3406C>T|p.Leu1136Leu |
S43 |
3 | BAA06g00020 | A06 | 36977 | C | T | missense_variant | MODERATE | c.3148G>A|p.Asp1050Asn |
S61 |
4 | BAA06g00020 | A06 | 38313 | G | A | stop_gained | HIGH | c.2527C>T|p.Arg843* |
S62 |
5 | BAA06g00020 | A06 | 38609 | G | A | intron_variant | MODIFIER | c.2385+40C>T| |
S200 |
6 | BAA06g00020 | A06 | 38759 | G | A | missense_variant | MODERATE | c.2275C>T|p.His759Tyr |
S173 |
7 | BAA06g00020 | A06 | 38937 | C | T | missense_variant | MODERATE | c.2170G>A|p.Val724Ile |
S122 |
8 | BAA06g00020 | A06 | 38940 | G | A | synonymous_variant | LOW | c.2167C>T|p.Leu723Leu |
S151 S166 S167 S236 S257 S262 S263 |
9 | BAA06g00020 | A06 | 38995 | G | A | intron_variant | MODIFIER | c.2127-15C>T| |
S245 |
10 | BAA06g00020 | A06 | 41759 | C | T | stop_gained | HIGH | c.1211G>A|p.Trp404* |
S172 S217 |
11 | BAA06g00020 | A06 | 42713 | G | A | missense_variant | MODERATE | c.742C>T|p.Leu248Phe |
S231 |
12 | BAA06g00020 | A06 | 42938 | G | A | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S275 |
13 | BAA06g00020 | A06 | 43015 | G | A | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S240 |
14 | BAA06g00020 | A06 | 43061 | C | T | missense_variant | MODERATE | c.394G>A|p.Asp132Asn |
S297 |
15 | BAA06g00020 | A06 | 43218 | G | A | synonymous_variant | LOW | c.237C>T|p.Leu79Leu |
S237 |
16 | BAA06g00020 | A06 | 43505 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S127 |
17 | BAA06g00020 | A06 | 45899 | G | A | upstream_gene_variant | MODIFIER | c.-2445C>T| |
S170 |
18 | BAA06g00020 | A06 | 48065 | C | T | upstream_gene_variant | MODIFIER | c.-4611G>A| |
S149 |
19 | BAA06g00020 | A06 | 48206 | C | T | upstream_gene_variant | MODIFIER | c.-4752G>A| |
S99 |