| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 138401 | BAA10g23880 | A10 | 19901984 | C | T | synonymous_variant | LOW | c.138C>T|p.Tyr46Tyr |
S122 |
| 138402 | BAA10g23880 | A10 | 19902498 | C | T | missense_variant | MODERATE | c.386C>T|p.Ala129Val |
S46 |
| 138403 | BAA10g23880 | A10 | 19904075 | C | T | synonymous_variant | LOW | c.1098C>T|p.Phe366Phe |
S26 |
| 138404 | BAA10g23880 | A10 | 19904091 | C | T | missense_variant | MODERATE | c.1114C>T|p.Pro372Ser |
S5 |
| 138405 | BAA10g23880 | A10 | 19904151 | C | T | missense_variant | MODERATE | c.1174C>T|p.Pro392Ser |
S68 |
| 138406 | BAA10g23870 | A10 | 19904498 | C | T | upstream_gene_variant | MODIFIER | c.-3752G>A| |
S177 |
| 138407 | BAA10g23880 | A10 | 19904582 | C | T | synonymous_variant | LOW | c.1425C>T|p.Tyr475Tyr |
S209 |
| 138408 | BAA10g23870 | A10 | 19905107 | C | T | upstream_gene_variant | MODIFIER | c.-4361G>A| |
S36 |
| 138409 | BAA10g23870 | A10 | 19905238 | C | T | upstream_gene_variant | MODIFIER | c.-4492G>A| |
S296 |
| 138410 | BAA10g23870 | A10 | 19905255 | G | A | upstream_gene_variant | MODIFIER | c.-4509C>T| |
S280 |
| 138411 | BAA10g23890 | A10 | 19906249 | C | T | missense_variant | MODERATE | c.602G>A|p.Arg201Lys |
S244 |
| 138412 | BAA10g23890 | A10 | 19907027 | G | A | synonymous_variant | LOW | c.204C>T|p.Ser68Ser |
S205 |
| 138413 | BAA10g23890 | A10 | 19907197 | C | T | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S161 |
| 138414 | BAA10g23890 | A10 | 19907295 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S192 |
| 138415 | BAA10g23890 | A10 | 19907689 | G | A | upstream_gene_variant | MODIFIER | c.-459C>T| |
S95 |
| 138416 | BAA10g23900 | A10 | 19909036 | G | A | missense_variant | MODERATE | c.1103C>T|p.Ser368Phe |
S134 |
| 138417 | BAA10g23900 | A10 | 19909077 | C | T | synonymous_variant | LOW | c.1062G>A|p.Gln354Gln |
S230 |
| 138418 | BAA10g23890 | A10 | 19909773 | C | T | upstream_gene_variant | MODIFIER | c.-2543G>A| |
S129 |
| 138419 | BAA10g23900 | A10 | 19910517 | G | A | missense_variant | MODERATE | c.334C>T|p.Leu112Phe |
S264 |
| 138420 | BAA10g23910 | A10 | 19912588 | C | T | missense_variant | MODERATE | c.67C>T|p.Arg23Trp |
S98 |
| 138421 | BAA10g23910 | A10 | 19912590 | G | A | synonymous_variant | LOW | c.69G>A|p.Arg23Arg |
S192 |
| 138422 | BAA10g23910 | A10 | 19912657 | C | T | missense_variant | MODERATE | c.136C>T|p.Pro46Ser |
S13 |
| 138423 | BAA10g23900 | A10 | 19913093 | C | T | upstream_gene_variant | MODIFIER | c.-2158G>A| |
S210 |
| 138424 | BAA10g23920 | A10 | 19914245 | G | A | synonymous_variant | LOW | c.471C>T|p.Thr157Thr |
S180 |
| 138425 | BAA10g23900 | A10 | 19915784 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S121 |