| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 90551 | BAA10g00620 | A10 | 302256 | C | T | missense_variant | MODERATE | c.1511C>T|p.Ser504Phe |
S60 |
| 90552 | BAA10g00620 | A10 | 302678 | G | A | missense_variant | MODERATE | c.1933G>A|p.Val645Met |
S217 |
| 90553 | BAA10g00620 | A10 | 302705 | G | A | missense_variant | MODERATE | c.1960G>A|p.Glu654Lys |
S284 |
| 90554 | BAA10g00620 | A10 | 303486 | G | A | missense_variant | MODERATE | c.2480G>A|p.Gly827Glu |
S136 |
| 90555 | BAA10g00620 | A10 | 303648 | C | T | missense_variant | MODERATE | c.2534C>T|p.Ser845Phe |
S104 |
| 90556 | BAA10g00630 | A10 | 303719 | G | A | downstream_gene_variant | MODIFIER | c.*4184C>T| |
S151 |
| 90557 | BAA10g00630 | A10 | 304013 | C | T | downstream_gene_variant | MODIFIER | c.*3890G>A| |
S165 |
| 90558 | BAA10g00620 | A10 | 304484 | C | T | missense_variant | MODERATE | c.2975C>T|p.Ser992Phe |
S165 |
| 90559 | BAA10g00620 | A10 | 305369 | C | T | missense_variant | MODERATE | c.3458C>T|p.Ser1153Phe |
S54 |
| 90560 | BAA10g00620 | A10 | 305544 | G | A | synonymous_variant | LOW | c.3633G>A|p.Glu1211Glu |
S15 S3 |
| 90561 | BAA10g00620 | A10 | 305809 | G | A | missense_variant | MODERATE | c.3898G>A|p.Ala1300Thr |
S65 |
| 90562 | BAA10g00620 | A10 | 306445 | G | A | missense_variant | MODERATE | c.4534G>A|p.Glu1512Lys |
S48 |
| 90563 | BAA10g00640 | A10 | 307707 | C | T | upstream_gene_variant | MODIFIER | c.-3215C>T| |
S269 |
| 90564 | BAA10g00630 | A10 | 308498 | G | A | missense_variant | MODERATE | c.125C>T|p.Ser42Phe |
S179 |
| 90565 | BAA10g00630 | A10 | 308951 | T | A | upstream_gene_variant | MODIFIER | c.-329A>T| |
S63 |
| 90566 | BAA10g00630 | A10 | 309338 | C | T | upstream_gene_variant | MODIFIER | c.-716G>A| |
S110 |
| 90567 | BAA10g00630 | A10 | 309690 | C | T | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S113 |
| 90568 | BAA10g00630 | A10 | 309943 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S197 |
| 90569 | BAA10g00630 | A10 | 312282 | G | A | upstream_gene_variant | MODIFIER | c.-3660C>T| |
S172 S217 |
| 90570 | BAA10g00630 | A10 | 312538 | G | A | upstream_gene_variant | MODIFIER | c.-3916C>T| |
S158 |
| 90571 | BAA10g00650 | A10 | 318896 | C | T | downstream_gene_variant | MODIFIER | c.*1144G>A| |
S152 |
| 90572 | BAA10g00650 | A10 | 319388 | G | A | downstream_gene_variant | MODIFIER | c.*652C>T| |
S236 |
| 90573 | BAA10g00650 | A10 | 319684 | G | A | downstream_gene_variant | MODIFIER | c.*356C>T| |
S71 |
| 90574 | BAA10g00650 | A10 | 320187 | C | T | synonymous_variant | LOW | c.1299G>A|p.Pro433Pro |
S199 |
| 90575 | BAA10g00650 | A10 | 320435 | C | T | missense_variant | MODERATE | c.1051G>A|p.Asp351Asn |
S177 |