| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141501 | BAA10g26530 | A10 | 21004069 | C | T | stop_gained | HIGH | c.817C>T|p.Gln273* |
S78 |
| 141502 | BAA10g26530 | A10 | 21004090 | C | T | stop_gained | HIGH | c.838C>T|p.Gln280* |
S218 |
| 141503 | BAA10g26530 | A10 | 21005424 | G | A | missense_variant | MODERATE | c.1771G>A|p.Ala591Thr |
S134 |
| 141504 | BAA10g26530 | A10 | 21005446 | C | T | missense_variant | MODERATE | c.1793C>T|p.Thr598Ile |
S167 |
| 141505 | BAA10g26540 | A10 | 21005572 | C | T | upstream_gene_variant | MODIFIER | c.-1497C>T| |
S36 |
| 141506 | BAA10g26540 | A10 | 21005754 | C | T | upstream_gene_variant | MODIFIER | c.-1315C>T| |
S8 |
| 141507 | BAA10g26540 | A10 | 21006001 | G | A | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S127 |
| 141508 | BAA10g26540 | A10 | 21006598 | G | A | upstream_gene_variant | MODIFIER | c.-471G>A| |
S250 |
| 141509 | BAA10g26540 | A10 | 21006890 | C | T | upstream_gene_variant | MODIFIER | c.-179C>T| |
S148 S210 S30 S31 |
| 141510 | BAA10g26540 | A10 | 21007202 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S119 |
| 141511 | BAA10g26540 | A10 | 21007209 | C | T | synonymous_variant | LOW | c.141C>T|p.Thr47Thr |
S38 |
| 141512 | BAA10g26540 | A10 | 21007581 | G | A | synonymous_variant | LOW | c.513G>A|p.Lys171Lys |
S231 |
| 141513 | BAA10g26540 | A10 | 21008233 | G | A | missense_variant | MODERATE | c.1165G>A|p.Ala389Thr |
S41 |
| 141514 | BAA10g26540 | A10 | 21008328 | G | A | synonymous_variant | LOW | c.1260G>A|p.Glu420Glu |
S207 |
| 141515 | BAA10g26540 | A10 | 21008584 | G | A | missense_variant | MODERATE | c.1516G>A|p.Gly506Arg |
S239 |
| 141516 | BAA10g26540 | A10 | 21009223 | C | T | synonymous_variant | LOW | c.2007C>T|p.Phe669Phe |
S301 S304 |
| 141517 | BAA10g26540 | A10 | 21009620 | G | A | splice_donor_variant&intron_variant | HIGH | c.2163+1G>A| |
S77 |
| 141518 | BAA10g26540 | A10 | 21010619 | G | A | intron_variant | MODIFIER | c.2553-37G>A| |
S226 |
| 141519 | BAA10g26550 | A10 | 21012329 | G | A | upstream_gene_variant | MODIFIER | c.-4543G>A| |
S17 |
| 141520 | BAA10g26550 | A10 | 21013366 | C | T | upstream_gene_variant | MODIFIER | c.-3506C>T| |
S98 |
| 141521 | BAA10g26550 | A10 | 21014162 | G | A | upstream_gene_variant | MODIFIER | c.-2710G>A| |
S122 |
| 141522 | BAA10g26550 | A10 | 21014291 | G | A | upstream_gene_variant | MODIFIER | c.-2581G>A| |
S183 |
| 141523 | BAA10g26550 | A10 | 21015618 | G | A | upstream_gene_variant | MODIFIER | c.-1254G>A| |
S175 |
| 141524 | BAA10g26550 | A10 | 21017565 | G | A | synonymous_variant | LOW | c.438G>A|p.Glu146Glu |
S81 S85 |
| 141525 | BAA10g26550 | A10 | 21018079 | G | A | synonymous_variant | LOW | c.786G>A|p.Val262Val |
S109 |