| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 99401 | BAA10g06520 | A10 | 3390551 | G | A | upstream_gene_variant | MODIFIER | c.-1406C>T| |
S66 |
| 99402 | BAA10g06520 | A10 | 3391195 | G | A | upstream_gene_variant | MODIFIER | c.-2050C>T| |
S53 |
| 99403 | BAA10g06520 | A10 | 3392125 | C | T | upstream_gene_variant | MODIFIER | c.-2980G>A| |
S263 |
| 99404 | BAA10g06520 | A10 | 3393898 | G | A | upstream_gene_variant | MODIFIER | c.-4753C>T| |
S57 |
| 99405 | BAA10g06520 | A10 | 3393945 | A | G | upstream_gene_variant | MODIFIER | c.-4800T>C| |
S175 |
| 99406 | BAA10g06530 | A10 | 3395228 | C | T | missense_variant | MODERATE | c.133C>T|p.Arg45Cys |
S177 |
| 99407 | BAA10g06530 | A10 | 3395251 | C | T | synonymous_variant | LOW | c.156C>T|p.Arg52Arg |
S177 |
| 99408 | BAA10g06530 | A10 | 3396812 | C | T | downstream_gene_variant | MODIFIER | c.*126C>T| |
S263 |
| 99409 | BAA10g06530 | A10 | 3397290 | C | T | downstream_gene_variant | MODIFIER | c.*604C>T| |
S155 S211 |
| 99410 | BAA10g06530 | A10 | 3398342 | C | T | downstream_gene_variant | MODIFIER | c.*1656C>T| |
S132 S137 S215 |
| 99411 | BAA10g06530 | A10 | 3398365 | G | A | downstream_gene_variant | MODIFIER | c.*1679G>A| |
S207 |
| 99412 | BAA10g06540 | A10 | 3399286 | C | T | missense_variant | MODERATE | c.886G>A|p.Gly296Arg |
S242 |
| 99413 | BAA10g06540 | A10 | 3399394 | C | T | missense_variant | MODERATE | c.778G>A|p.Asp260Asn |
S233 |
| 99414 | BAA10g06540 | A10 | 3399456 | C | T | missense_variant | MODERATE | c.716G>A|p.Gly239Glu |
S11 |
| 99415 | BAA10g06540 | A10 | 3399557 | G | A | synonymous_variant | LOW | c.615C>T|p.Asp205Asp |
S97 |
| 99416 | BAA10g06540 | A10 | 3400270 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S274 |
| 99417 | BAA10g06540 | A10 | 3400408 | G | A | upstream_gene_variant | MODIFIER | c.-23C>T| |
S292 |
| 99418 | BAA10g06550 | A10 | 3401204 | C | T | missense_variant | MODERATE | c.964G>A|p.Ala322Thr |
S249 |
| 99419 | BAA10g06550 | A10 | 3401669 | C | T | missense_variant | MODERATE | c.499G>A|p.Glu167Lys |
S144 |
| 99420 | BAA10g06550 | A10 | 3402002 | G | A | synonymous_variant | LOW | c.426C>T|p.Leu142Leu |
S241 |
| 99421 | BAA10g06550 | A10 | 3402230 | C | T | synonymous_variant | LOW | c.198G>A|p.Lys66Lys |
S229 |
| 99422 | BAA10g06550 | A10 | 3402395 | G | A | missense_variant | MODERATE | c.107C>T|p.Thr36Ile |
S245 |
| 99423 | BAA10g06540 | A10 | 3403829 | C | T | upstream_gene_variant | MODIFIER | c.-3444G>A| |
S131 |
| 99424 | BAA10g06540 | A10 | 3403876 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S159 S243 S299 |
| 99425 | BAA10g06540 | A10 | 3403998 | T | A | upstream_gene_variant | MODIFIER | c.-3613A>T| |
S26 |