| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 122401 | BAA10g12760 | A10 | 14104443 | G | A | synonymous_variant | LOW | c.1476C>T|p.Arg492Arg |
S192 |
| 122402 | BAA10g12760 | A10 | 14104899 | G | A | synonymous_variant | LOW | c.1170C>T|p.Leu390Leu |
S289 |
| 122403 | BAA10g12760 | A10 | 14105053 | G | A | missense_variant | MODERATE | c.1016C>T|p.Ser339Phe |
S261 |
| 122404 | BAA10g12760 | A10 | 14105087 | C | T | missense_variant | MODERATE | c.982G>A|p.Asp328Asn |
S305 |
| 122405 | BAA10g12760 | A10 | 14106429 | C | T | intron_variant | MODIFIER | c.785+709G>A| |
S180 |
| 122406 | BAA10g12760 | A10 | 14107550 | C | T | missense_variant | MODERATE | c.460G>A|p.Val154Ile |
S12 |
| 122407 | BAA10g12760 | A10 | 14108052 | G | A | upstream_gene_variant | MODIFIER | c.-43C>T| |
S59 |
| 122408 | BAA10g12760 | A10 | 14108200 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S218 |
| 122409 | BAA10g12760 | A10 | 14108830 | G | A | upstream_gene_variant | MODIFIER | c.-821C>T| |
S35 |
| 122410 | BAA10g12760 | A10 | 14109289 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S261 |
| 122411 | BAA10g12760 | A10 | 14109632 | G | A | upstream_gene_variant | MODIFIER | c.-1623C>T| |
S217 |
| 122412 | BAA10g12760 | A10 | 14110204 | C | T | upstream_gene_variant | MODIFIER | c.-2195G>A| |
S224 |
| 122413 | BAA10g12760 | A10 | 14110474 | G | A | upstream_gene_variant | MODIFIER | c.-2465C>T| |
S1 S90 |
| 122414 | BAA10g12760 | A10 | 14111509 | G | A | upstream_gene_variant | MODIFIER | c.-3500C>T| |
S1 S90 |
| 122415 | BAA10g12770 | A10 | 14111676 | C | T | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S142 |
| 122416 | BAA10g12760 | A10 | 14112189 | G | A | upstream_gene_variant | MODIFIER | c.-4180C>T| |
S150 |
| 122417 | BAA10g12760 | A10 | 14112624 | G | A | upstream_gene_variant | MODIFIER | c.-4615C>T| |
S129 |
| 122418 | BAA10g12770 | A10 | 14115587 | C | T | upstream_gene_variant | MODIFIER | c.-3719G>A| |
S153 S213 |
| 122419 | BAA10g12780 | A10 | 14117547 | C | T | missense_variant | MODERATE | c.622G>A|p.Glu208Lys |
S266 |
| 122420 | BAA10g12780 | A10 | 14118523 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S62 |
| 122421 | BAA10g12780 | A10 | 14119297 | C | T | upstream_gene_variant | MODIFIER | c.-534G>A| |
S177 |
| 122422 | BAA10g12790 | A10 | 14119430 | C | T | synonymous_variant | LOW | c.1764G>A|p.Glu588Glu |
S54 |
| 122423 | BAA10g12790 | A10 | 14120691 | C | T | missense_variant | MODERATE | c.503G>A|p.Arg168Lys |
S142 |
| 122424 | BAA10g12790 | A10 | 14120774 | G | A | synonymous_variant | LOW | c.420C>T|p.Val140Val |
S207 |
| 122425 | BAA10g12780 | A10 | 14121673 | G | A | upstream_gene_variant | MODIFIER | c.-2910C>T| |
S39 |