Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07060 | A10 | 3881640 | C | T | upstream_gene_variant | MODIFIER | c.-815C>T| |
S123 |
2 | BAA10g07060 | A10 | 3882525 | G | A | missense_variant | MODERATE | c.71G>A|p.Gly24Glu |
S95 |
3 | BAA10g07060 | A10 | 3882648 | C | T | intron_variant | MODIFIER | c.168+26C>T| |
S270 |
4 | BAA10g07060 | A10 | 3882854 | C | T | missense_variant | MODERATE | c.310C>T|p.Pro104Ser |
S246 |
5 | BAA10g07060 | A10 | 3883339 | G | A | stop_gained | HIGH | c.722G>A|p.Trp241* |
S192 |
6 | BAA10g07060 | A10 | 3884364 | G | A | missense_variant | MODERATE | c.1660G>A|p.Glu554Lys |
S90 |
7 | BAA10g07060 | A10 | 3884793 | G | A | missense_variant | MODERATE | c.1977G>A|p.Met659Ile |
S237 |
8 | BAA10g07060 | A10 | 3885231 | C | T | intron_variant | MODIFIER | c.2191-50C>T| |
S88 |
9 | BAA10g07060 | A10 | 3885757 | C | T | missense_variant | MODERATE | c.2500C>T|p.Arg834Trp |
S191 |
10 | BAA10g07060 | A10 | 3899634 | G | A | missense_variant | MODERATE | c.11858G>A|p.Arg3953Gln |
S17 |
11 | BAA10g07060 | A10 | 3899659 | G | A | synonymous_variant | LOW | c.11883G>A|p.Lys3961Lys |
S267 |
12 | BAA10g07060 | A10 | 3899692 | C | T | synonymous_variant | LOW | c.11916C>T|p.Ser3972Ser |
S116 |
13 | BAA10g07060 | A10 | 3902641 | C | T | missense_variant | MODERATE | c.12809C>T|p.Pro4270Leu |
S175 |
14 | BAA10g07060 | A10 | 3902988 | C | T | stop_gained | HIGH | c.13156C>T|p.Gln4386* |
S159 S243 S299 |
15 | BAA10g07060 | A10 | 3903158 | G | A | stop_gained | HIGH | c.13326G>A|p.Trp4442* |
S67 |
16 | BAA10g07060 | A10 | 3903257 | G | A | missense_variant | MODERATE | c.13425G>A|p.Met4475Ile |
S296 |