| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 125201 | BAA10g14490 | A10 | 15176795 | G | A | synonymous_variant | LOW | c.105C>T|p.Cys35Cys |
S159 S243 |
| 125202 | BAA10g14490 | A10 | 15176997 | G | A | synonymous_variant | LOW | c.21C>T|p.Ser7Ser |
S4 |
| 125203 | BAA10g14500 | A10 | 15178030 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Phe |
S169 |
| 125204 | BAA10g14500 | A10 | 15178042 | G | A | missense_variant | MODERATE | c.38G>A|p.Gly13Glu |
S182 S75 S9 |
| 125205 | BAA10g14480 | A10 | 15178668 | C | T | upstream_gene_variant | MODIFIER | c.-4598G>A| |
S299 |
| 125206 | BAA10g14510 | A10 | 15181672 | C | T | missense_variant | MODERATE | c.634G>A|p.Val212Met |
S28 |
| 125207 | BAA10g14510 | A10 | 15181760 | G | A | synonymous_variant | LOW | c.546C>T|p.Ile182Ile |
S295 |
| 125208 | BAA10g14510 | A10 | 15182071 | G | A | missense_variant | MODERATE | c.325C>T|p.Leu109Phe |
S148 S30 S31 |
| 125209 | BAA10g14510 | A10 | 15182256 | G | A | missense_variant | MODERATE | c.140C>T|p.Ala47Val |
S203 |
| 125210 | BAA10g14520 | A10 | 15182808 | C | T | missense_variant | MODERATE | c.1363G>A|p.Val455Met |
S306 S308 |
| 125211 | BAA10g14520 | A10 | 15182996 | C | T | missense_variant | MODERATE | c.1175G>A|p.Gly392Glu |
S232 |
| 125212 | BAA10g14520 | A10 | 15183137 | C | T | missense_variant | MODERATE | c.1034G>A|p.Cys345Tyr |
S175 |
| 125213 | BAA10g14520 | A10 | 15183277 | C | T | synonymous_variant | LOW | c.894G>A|p.Lys298Lys |
S176 |
| 125214 | BAA10g14520 | A10 | 15183856 | G | A | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S25 |
| 125215 | BAA10g14520 | A10 | 15183979 | G | A | missense_variant | MODERATE | c.268C>T|p.Leu90Phe |
S9 |
| 125216 | BAA10g14520 | A10 | 15184095 | C | T | missense_variant | MODERATE | c.152G>A|p.Gly51Asp |
S152 |
| 125217 | BAA10g14510 | A10 | 15184416 | G | A | upstream_gene_variant | MODIFIER | c.-2021C>T| |
S18 |
| 125218 | BAA10g14510 | A10 | 15185892 | C | T | upstream_gene_variant | MODIFIER | c.-3497G>A| |
S28 |
| 125219 | BAA10g14510 | A10 | 15186488 | G | A | upstream_gene_variant | MODIFIER | c.-4093C>T| |
S80 |
| 125220 | BAA10g14530 | A10 | 15188424 | C | T | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S121 |
| 125221 | BAA10g14530 | A10 | 15188798 | C | T | missense_variant | MODERATE | c.1160C>T|p.Ser387Phe |
S229 |
| 125222 | BAA10g14530 | A10 | 15189474 | G | A | missense_variant&splice_region_variant | MODERATE | c.1654G>A|p.Gly552Arg |
S192 |
| 125223 | BAA10g14530 | A10 | 15189479 | C | T | splice_region_variant&intron_variant | LOW | c.1655+4C>T| |
S225 S73 |
| 125224 | BAA10g14540 | A10 | 15190956 | G | A | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S120 |
| 125225 | BAA10g14540 | A10 | 15190996 | G | A | synonymous_variant | LOW | c.144G>A|p.Arg48Arg |
S155 S211 |