| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141351 | BAA10g26360 | A10 | 20937032 | G | A | missense_variant | MODERATE | c.374C>T|p.Ser125Phe |
S143 |
| 141352 | BAA10g26360 | A10 | 20937335 | G | A | missense_variant | MODERATE | c.71C>T|p.Thr24Met |
S82 S92 |
| 141353 | BAA10g26350 | A10 | 20937774 | G | A | upstream_gene_variant | MODIFIER | c.-4024C>T| |
S32 |
| 141354 | BAA10g26350 | A10 | 20937965 | C | T | upstream_gene_variant | MODIFIER | c.-4215G>A| |
S166 |
| 141355 | BAA10g26360 | A10 | 20940434 | C | T | upstream_gene_variant | MODIFIER | c.-3029G>A| |
S47 |
| 141356 | BAA10g26370 | A10 | 20943020 | C | T | downstream_gene_variant | MODIFIER | c.*901G>A| |
S148 S210 S30 S31 |
| 141357 | BAA10g26370 | A10 | 20944090 | G | A | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S136 |
| 141358 | BAA10g26370 | A10 | 20944266 | C | T | synonymous_variant | LOW | c.60G>A|p.Arg20Arg |
S210 S225 |
| 141359 | BAA10g26370 | A10 | 20945440 | G | A | upstream_gene_variant | MODIFIER | c.-1115C>T| |
S270 |
| 141360 | BAA10g26370 | A10 | 20946414 | G | A | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S100 |
| 141361 | BAA10g26370 | A10 | 20946468 | C | T | upstream_gene_variant | MODIFIER | c.-2143G>A| |
S162 |
| 141362 | BAA10g26370 | A10 | 20947852 | C | T | upstream_gene_variant | MODIFIER | c.-3527G>A| |
S277 |
| 141363 | BAA10g26370 | A10 | 20948393 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S168 |
| 141364 | BAA10g26370 | A10 | 20949177 | C | T | upstream_gene_variant | MODIFIER | c.-4852G>A| |
S238 |
| 141365 | BAA10g26380 | A10 | 20951975 | G | A | upstream_gene_variant | MODIFIER | c.-537G>A| |
S298 |
| 141366 | BAA10g26390 | A10 | 20953074 | G | A | upstream_gene_variant | MODIFIER | c.-2863G>A| |
S71 |
| 141367 | BAA10g26380 | A10 | 20953664 | C | T | missense_variant | MODERATE | c.613C>T|p.Arg205Cys |
S162 |
| 141368 | BAA10g26390 | A10 | 20955975 | G | A | missense_variant | MODERATE | c.39G>A|p.Met13Ile |
S265 |
| 141369 | BAA10g26400 | A10 | 20957784 | C | T | upstream_gene_variant | MODIFIER | c.-663C>T| |
S204 |
| 141370 | BAA10g26400 | A10 | 20958451 | G | A | missense_variant | MODERATE | c.5G>A|p.Arg2Lys |
S70 |
| 141371 | BAA10g26400 | A10 | 20958505 | C | T | missense_variant | MODERATE | c.59C>T|p.Ala20Val |
S103 |
| 141372 | BAA10g26400 | A10 | 20958591 | C | T | missense_variant | MODERATE | c.145C>T|p.Pro49Ser |
S153 S213 |
| 141373 | BAA10g26410 | A10 | 20958711 | C | T | upstream_gene_variant | MODIFIER | c.-3179C>T| |
S36 |
| 141374 | BAA10g26410 | A10 | 20960342 | G | A | upstream_gene_variant | MODIFIER | c.-1548G>A| |
S179 |
| 141375 | BAA10g26410 | A10 | 20960685 | C | T | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S68 |